U.S. patent application number 17/247834 was filed with the patent office on 2022-09-01 for boron-containing small molecules.
This patent application is currently assigned to Bill & Melinda Gates Foundation. The applicant listed for this patent is Bill & Melinda Gates Foundation. Invention is credited to Robert T. JACOBS, Xianfeng LI, Christopher S. LUNDE, Yasheen ZHOU.
Application Number | 20220273683 17/247834 |
Document ID | / |
Family ID | 1000006322392 |
Filed Date | 2022-09-01 |
United States Patent
Application |
20220273683 |
Kind Code |
A1 |
LI; Xianfeng ; et
al. |
September 1, 2022 |
BORON-CONTAINING SMALL MOLECULES
Abstract
Compounds, pharmaceutical formulations, and methods of treating
bacterial infections are disclosed.
Inventors: |
LI; Xianfeng; (Cupertino,
CA) ; LUNDE; Christopher S.; (Belmont, CA) ;
JACOBS; Robert T.; (Wake Forest, NC) ; ZHOU;
Yasheen; (Moraga, CA) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Bill & Melinda Gates Foundation |
Seattle |
WA |
US |
|
|
Assignee: |
Bill & Melinda Gates
Foundation
Seattle
WA
|
Family ID: |
1000006322392 |
Appl. No.: |
17/247834 |
Filed: |
December 24, 2020 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
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16840239 |
Apr 3, 2020 |
10874679 |
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17247834 |
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16081904 |
Sep 1, 2018 |
10611781 |
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PCT/US2017/019658 |
Feb 27, 2017 |
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16840239 |
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62302591 |
Mar 2, 2016 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
A61K 45/06 20130101;
A61K 31/69 20130101; C07F 5/027 20130101; A61P 31/04 20180101 |
International
Class: |
A61K 31/69 20060101
A61K031/69; A61P 31/04 20060101 A61P031/04; C07F 5/02 20060101
C07F005/02; A61K 45/06 20060101 A61K045/06 |
Claims
1. A compound, or a salt or a hydrate or a solvate thereof, having
a structure which is: ##STR00152## wherein W is H or a bond to X; X
is ##STR00153## wherein R.sup.a and R.sup.b are each independently
selected from the group consisting of R.sup.15, --OR.sup.15,
--NR.sup.15R.sup.16, --SR.sup.15, --S(O)R.sup.15,
--S(O).sub.2R.sup.15, --S(O).sub.2NR.sup.15R.sup.16,
--C(O)R.sup.15, --C(O)OR.sup.15, and --C(O)NR.sup.15R.sup.16
wherein R.sup.15 and R.sup.16 are each independently selected from
the group consisting of H, halogen, cyano, nitro, --OR.sup.17,
--NR.sup.17R.sup.18, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, and
substituted or unsubstituted heteroaryl wherein R.sup.17 and
R.sup.18 are each independently selected from the group consisting
of H, substituted or unsubstituted alkyl, substituted or
unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl,
substituted or unsubstituted heterocycloalkyl, substituted or
unsubstituted aryl, and substituted or unsubstituted heteroaryl and
wherein R.sup.15 and R.sup.16, and/or R.sup.17 and R.sup.18, along
with the nitrogen to which they are connected, are optionally
joined to form a substituted or unsubstituted 4- to 8-membered ring
with the proviso that R.sup.a and R.sup.b are not both H; or X is
##STR00154## wherein R.sup.c is --OR.sup.15, --NR.sup.15R.sup.16,
--SR.sup.15, --S(O)R.sup.15, --S(O).sub.2R.sup.15,
--S(O).sub.2NR.sup.15R.sup.16, --C(O)R.sup.15, --C(O)OR.sup.15, and
--C(O)NR.sup.15R.sup.16 wherein R.sup.15 and R.sup.16 are each
independently selected from the group consisting of H, halogen,
cyano, nitro, substituted or unsubstituted alkyl, substituted or
unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl,
substituted or unsubstituted heterocycloalkyl, substituted or
unsubstituted aryl, and substituted or unsubstituted heteroaryl and
wherein R.sup.15 and R.sup.16, along with the nitrogen to which
they are connected, are optionally joined to form a substituted or
unsubstituted 4- to 8-membered ring or X is ##STR00155## wherein
R.sup.d and R.sup.e are each independently selected from the group
consisting of H, halogen, cyano, nitro, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl, --OR.sup.15,
--NR.sup.15R.sup.16, --SR.sup.15, --S(O)R.sup.15,
--S(O).sub.2R.sup.15, --S(O).sub.2NR.sup.15R.sup.16,
--C(O)R.sup.15, --C(O)OR.sup.15, and --C(O)NR.sup.15R.sup.16
wherein R.sup.15 and R.sup.16 are each independently selected from
the group consisting of H, halogen, cyano, nitro, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl and wherein R.sup.d and
R.sup.e, along with the atom to which they are connected, are
optionally joined to form a substituted or unsubstituted 3- to
8-membered ring and wherein R.sup.15 and R.sup.16, along with the
nitrogen to which they are connected, are optionally joined to form
a substituted or unsubstituted 4- to 8-membered ring with the
proviso that R.sup.d and R.sup.e are not both H wherein X
optionally comprises an attachment point to W; Y is selected from
the group consisting of a bond, --O--, --S--, --NH--, substituted
or unsubstituted alkylene, and substituted or unsubstituted
heteroalkylene; and Z is a substituted or unsubstituted
heterocyclic ring or ring system containing at least one endocyclic
boron.
2. The compound of claim 1, or a salt or a hydrate or a solvate
thereof, wherein said X is ##STR00156## wherein R.sup.15 is
selected from the group consisting of H, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl.
3. The compound of claim 1, or a salt or a hydrate or a solvate
thereof, wherein said X is ##STR00157## wherein R.sup.15 and
R.sup.16 are each independently selected from the group consisting
of H, --OR.sup.17, --NR.sup.17R.sup.18, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl wherein R.sup.17 and
R.sup.18 are each independently selected from the group consisting
of H, substituted or unsubstituted alkyl, substituted or
unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl,
substituted or unsubstituted heterocycloalkyl, substituted or
unsubstituted aryl, and substituted or unsubstituted heteroaryl and
wherein R.sup.15 and R.sup.16, and/or R.sup.17 and R.sup.18, along
with the nitrogen to which they are connected, are optionally
joined to form a substituted or unsubstituted 4- to 8-membered
ring.
4. The compound of claim 1, or a salt or a hydrate or a solvate
thereof, wherein said X is ##STR00158## wherein R.sup.c is selected
from the group consisting of H, substituted or unsubstituted alkyl,
and --OR.sup.15 wherein R.sup.15 is H or substituted or
unsubstituted alkyl.
5. The compound of claim 1, or a salt or a hydrate or a solvate
thereof, wherein said X is ##STR00159## wherein R.sup.d is selected
from the group consisting of halogen, substituted or unsubstituted
alkyl, substituted or unsubstituted heterocycloalkyl, substituted
or unsubstituted aryl, --OR.sup.15, --SR.sup.15, --S(O)R.sup.15,
--NR.sup.15R.sup.16, --C(O)R.sup.15, --CH.sub.2C(O)OR.sup.15, and
--CH.sub.2C(O)NR.sup.15R.sup.16 wherein R.sup.15 and R.sup.16 are
each independently selected from the group consisting of H,
substituted or unsubstituted alkyl, substituted or unsubstituted
heteroalkyl, substituted or unsubstituted cycloalkyl, substituted
or unsubstituted heterocycloalkyl, substituted or unsubstituted
aryl, and substituted or unsubstituted heteroaryl and wherein
R.sup.15 and R.sup.16, along with the nitrogen to which they are
connected, are optionally joined to form a substituted or
unsubstituted 4- to 8-membered ring.
6. The compound of claim 5, or a salt or a hydrate or a solvate
thereof, wherein R.sup.d comprises said attachment point to W.
7. The compound of claim 1, or a salt or a hydrate or a solvate
thereof, wherein said Y is *--OCH.sub.2-- or *--SCH.sub.2-- or
*--NHCH.sub.2-- or *--CH.sub.2NH-- or *--C(O)NH--, wherein *
represents the attachment point to said Z.
8. The compound of claim 1, or a salt or a hydrate or a solvate
thereof, wherein said Z is selected from the group consisting of
substituted or unsubstituted benzoxaborole, substituted or
unsubstituted pyridinyloxaborole, substituted or unsubstituted
benzoxaborininol, substituted or unsubstituted benzoxazaborininol,
substituted or unsubstituted benzodiazaborininol, and substituted
or unsubstituted oxaborole.
9. The compound of claim 8, or a salt or a hydrate or a solvate
thereof, wherein said Z is ##STR00160## wherein R.sup.3, R.sup.3a,
R.sup.4, R.sup.5, and R.sup.7 are each independently selected from
the group consisting of R.sup.10, --OR.sup.10, --NR.sup.10R.sup.11,
--SR.sup.10, --S(O)R.sup.10, --S(O).sub.2R.sup.10,
--S(O).sub.2NR.sup.10R.sup.11, --C(O)R.sup.10, --C(O)OR.sup.10, and
--C(O)NR.sup.10R.sup.11 wherein R.sup.10 and R.sup.11 are each
independently selected from the group consisting of H, halogen,
cyano, nitro, substituted or unsubstituted alkyl, substituted or
unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl,
substituted or unsubstituted heterocycloalkyl, substituted or
unsubstituted aryl, and substituted or unsubstituted
heteroaryl.
10. The compound of claim 9, or a salt or a hydrate or a solvate
thereof, wherein said Z is ##STR00161## wherein R.sup.4, R.sup.5,
and R.sup.7 are each independently selected from the group
consisting of R.sup.10, --OR.sup.10, --NR.sup.10R.sup.11, wherein
R.sup.10 and R.sup.11 are each independently selected from the
group consisting of H, halogen, cyano, nitro, substituted or
unsubstituted alkyl, and substituted or unsubstituted
heteroalkyl.
11. The compound of claim 10, or a salt or a hydrate or a solvate
thereof, wherein said Z is ##STR00162##
12. A combination comprising the compound of claim 1, or a
pharmaceutically acceptable salt thereof, together with at least
one other therapeutically active agent.
13. The combination of claim 12, or a pharmaceutically acceptable
salt or a hydrate or a solvate thereof, wherein the other
therapeutically active agent is an anti-bacterial agent.
14. A pharmaceutical formulation comprising: a) the compound of
claim 1, or a pharmaceutically acceptable salt or a hydrate or a
solvate thereof, and b) a pharmaceutically acceptable
excipient.
15. A method of inhibiting protein synthesis in a bacteria, the
method comprising contacting the bacteria with the compound of
claim 1, or a pharmaceutically acceptable salt or a hydrate or a
solvate thereof, thereby inhibiting protein synthesis in the
bacteria.
16. A method of inhibiting the growth of and/or killing a bacteria,
the method comprising contacting the bacteria with the compound of
claim 1, or a pharmaceutically acceptable salt or a hydrate or a
solvate thereof, thereby inhibiting the growth of and/or killing
the bacteria.
17. The method of claim 15, wherein the bacteria is
Gram-positive.
18. The method of claim 17, wherein the bacteria is selected from
the group consisting of Staphylococcus aureus, Streptococcus
pneumoniae, methicillin-resistant Staphylococcus aureus, Wolbachia
pipientis, and bacteria of the Wolbachia genus.
19. A method of treating a disease in an animal, the method
comprising administering to the animal a therapeutically effective
amount of the compound of claim 1, or a pharmaceutically acceptable
salt or a hydrate or a solvate thereof, thereby treating the
disease.
20. The method of claim 19, wherein the disease is associated with
a Gram-positive bacteria.
21. The method of claim 19, wherein the disease is selected from
the group consisting of pneumonia, hospital-acquired pneumonia,
hospital-associated pneumonia, community-acquired pneumonia, acute
bacterial skin and skin-structure infection (ABSSSI), bacteremia,
endocarditis, osteomyelitis, gastroenteritis, toxic shock syndrome,
meningitis, septic arthritis, urinary tract infection, skin and
skin-structure infection, strep throat, necrotizing fasciitis,
otitis media, sinusitis, actinomycosis, diptheria, anthrax, food
poisoning, botulism, tetanus, gas gangrene, diarrhea, tuberculosis,
leprosy, candidiasis, aspergillosis, coccidioidomycosis,
cryptococcosis, histoplasmosis, blastomycosis,
paracoccidioidomycosis, zygomycosis, phaeohyphomycosis,
rhinosporidiosis, enterobiasis, filariasis, lymphatic filariasis,
bancroftian filariasis, subcutaneous filariasis, serious cavity
filariasis, elephantiasis, elephantiasis tropica, lymphadenitis,
lymphangitis, lymphedema, and onchocerciasis.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This is a continuation application of U.S. application Ser.
No. 16/840,239, filed Apr. 3, 2020 which is a continuation of
application of U.S. application Ser. No. 16/081,904, filed Sep. 1,
2018, now U.S. Pat. No. 10,611,781, issued Apr. 7, 2020, which is a
national phase application of International Patent Application No.
PCT/US2017/019658, filed Feb. 27, 2017, which claims the benefit of
U.S. Provisional Patent Application No. 62/302,591, filed Mar. 2,
2016, which is incorporated by reference in its entirety for all
purpose.
BACKGROUND OF THE INVENTION
[0002] The present invention relates to organic compounds, such as
pleuromutilins. Pleuromutilin, a compound having the following
formula:
##STR00001##
is a naturally occurring antibacterial, e.g. produced by the
basidomycetes Pleurotus mutilus and P. passeckerianus, see e.g. The
Merck Index, 13th edition, item 7617. Further modified
pleuromutilins are also known.
[0003] Surprisingly, it has now been discovered that certain
classes of pleuromutilins modified with boron are surprisingly
effective antibacterials. This, and other uses of these compounds,
are described herein.
SUMMARY OF THE INVENTION
[0004] In a first aspect, the invention provides a compound having
a structure which is a salt or a hydrate or a solvate thereof,
having a structure which is:
##STR00002##
wherein the variables are as defined herein.
[0005] In a second aspect, the invention provides a combination
comprising a compound of the invention together with at least one
other therapeutically active agent.
[0006] In a third aspect, the invention provides a pharmaceutical
formulation comprising: a) a compound of the invention; and b) a
pharmaceutically acceptable excipient.
[0007] In a fourth aspect, the invention provides a method of
inhibiting protein synthesis in a bacteria, the method comprising
contacting the bacteria with a compound of the invention, thereby
inhibiting protein synthesis in the bacteria.
[0008] In a fifth aspect, the invention provides a method of
inhibiting the growth and/or killing a bacteria, the method
comprising contacting the bacteria with the compound of the
invention, thereby inhibiting the growth and/or killing the
bacteria.
[0009] In a sixth aspect, the invention provides a method of
treating a microbial disease and/or a worm disease in an animal,
the method comprising administering to the animal a therapeutically
effective amount of a compound of the invention, thereby treating
the microbial disease and/or the worm disease.
DETAILED DESCRIPTION OF THE INVENTION
I. Definitions and Abbreviations
[0010] As used herein, the singular forms "a," "an", and "the"
include plural references unless the context clearly dictates
otherwise. For example, reference to "an active agent" includes a
single active agent as well as two or more different active agents
in combination. It is to be understood that present teaching is not
limited to the specific dosage forms, carriers, or the like,
disclosed herein and as such may vary.
[0011] The abbreviations used herein generally have their
conventional meaning within the chemical and biological arts.
[0012] The following abbreviations have been used: Ac is acetyl;
AcOH is acetic acid; ACTBr is cetyltrimethylammonium bromide; AIBN
is azobisisobutyronitrile or 2,2 azobisisobutyronitrile; aq. is
aqueous; Ar is aryl; B.sub.2pin.sub.2 is bis(pinacolato)diboron; Bn
is, in general, benzyl [see Cbz for one example of an exception];
(BnS).sub.2 is benzyl disulfide; BnSH is benzyl thiol or benzyl
mercaptan; BnBr is benzyl bromide; Boc is tert-butoxy carbonyl;
Boc.sub.2O is di-tert-butyl dicarbonate; Bz is, in general,
benzoyl; BzOOH is benzoyl peroxide; Cbz or Z is benzyloxycarbonyl
or carboxybenzyl; Cs.sub.2CO.sub.3 is cesium carbonate; CSA is
camphor sulfonic acid; CTAB is cetyltrimethylammonium bromide; Cy
is cyclohexyl; DABCO is 1,4-diazabicyclo[2.2.2]octane; DCM is
dichloromethane or methylene chloride; DHP is dihydropyran; DIAD is
diisopropyl azodicarboxylate; DIEA or DIPEA is
N,N-diisopropylethylamine; DMAP is 4-(dimethylamino)pyridine; DME
is 1,2-dimethoxyethane; DMF is N,N-dimethylformamide; DMSO is
dimethylsulfoxide; equiv or eq. is equivalent; EtOAc is ethyl
acetate; EtOH is ethanol; Et.sub.2O is diethyl ether; EDCI is
N-(3-dimethylaminopropyl)-N-ethylcarbodiimide hydrochloride; ELS is
evaporative light scattering; equiv or eq is equivalent; h is
hours; HATU is
O-(7-azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium
hexafluorophosphate; HOBt is N-hydroxybenzotriazole; HCl is
hydrochloric acid; HPLC is high pressure liquid chromatography;
ISCO Companion is automated flash chromatography equipment with
fraction analysis by UV absorption available from Presearch; KOAc
or AcOK is potassium acetate; K.sub.2CO.sub.3 is potassium
carbonate; LiAlH.sub.4 or LAH is lithium aluminum hydride; LDA is
lithium diisopropylamide; LHMDS is lithium bis(trimethylsilyl)
amide; KHMDS is potassium bis(trimethylsilyl) amide; LiOH is
lithium hydroxide; m-CPBA is 3-chloroperoxybenzoic acid; MeCN or
ACN is methyl cyanide or cyanomethane or ethanenitrile or
acetonitrile which are all names for the same compound; MeOH is
methanol; MgSO.sub.4 is magnesium sulfate; mins or min is minutes;
Mp or MP is melting point; NaCNBH.sub.3 is sodium cyanoborohydride;
NaOH is sodium hydroxide; Na.sub.2SO.sub.4 is sodium sulfate; NBS
is N-bromosuccinimide; NH.sub.4Cl is ammonium chloride; NIS is
N-iodosuccinimide; N.sub.2 is nitrogen; NMM is N-methylmorpholine;
n-BuLi is n-butyllithium; overnight is O/N; PdCl.sub.2(pddf) is
1,1'-Bis(diphenylphosphino) ferrocene]dichloropalladium(II); Pd/C
is the catalyst known as palladium on carbon; Pd.sub.2(dba).sub.3
is an organometallic catalyst known as tris(dibenzylideneacetone)
dipalladium(O); R.sup.a Ni or Raney Ni is Raney nickel; Ph is
phenyl; PMB is p-methoxybenzyl; PrOH is 1-propanol; iPrOH is
2-propanol; POCl.sub.3 is phosphorus chloride oxide; PTSA is
para-toluene sulfonic acid; Pyr. or Pyr or Py as used herein means
Pyridine; RT or rt or r.t. is room temperature; sat. is saturated;
Si-amine or Si--NH.sub.2 is amino-functionalized silica, available
from SiliCycle; Si-pyr is pyridyl-functionalized silica, available
from SiliCycle; TEA or Et.sub.3N is triethylamine; TFA is
trifluoroacetic acid; Tf.sub.2O is trifluoromethanesulfonic
anhydride; THE is tetrahydrofuran; TFAA is trifluoroacetic
anhydride; THP is tetrahydropyranyl; TMSI is trimethylsilyl iodide;
H.sub.2O is water; diNO.sub.2PhSO.sub.2Cl is dinitrophenyl sulfonyl
chloride; 3-F-4-NO.sub.2-PhSO.sub.2Cl is
3-fluoro-4-nitrophenylsulfonyl chloride;
2-MeO-4-NO.sub.2-PhSO.sub.2Cl is 2-methoxy-4-nitrophenylsulfonyl
chloride; and (EtO).sub.2POCH.sub.2COOEt is a triethylester of
phosphonoacetic acid known as triethyl phosphonoacetate.
[0013] "Compound of the invention," as used herein, refers to the
compounds discussed herein, salts (e.g. pharmaceutically acceptable
salts), prodrugs, solvates and hydrates of these compounds.
[0014] "Combination of the invention," as used herein, refers to
the compounds and antiinflammatories discussed herein as well as
acids, bases, salt forms (such as pharmaceutically acceptable
salts), prodrugs, solvates and hydrates of these compounds and
antiinflammatories.
[0015] "Boron containing compounds", as used herein, refers to the
compounds of the invention that contain boron as part of their
chemical formula.
[0016] The term "poly" as used herein means at least 2. For
example, a polyvalent metal ion is a metal ion having a valency of
at least 2.
[0017] "Moiety" refers to a radical of a molecule that is attached
to the remainder of the molecule.
[0018] The symbol , whether utilized as a bond or dis played
perpendicular to a bond, indicates the point at which the dis
played moiety is attached to the remainder of the molecule.
[0019] The term "alkyl," by itself or as part of another
substituent, means, unless otherwise stated, a straight or branched
chain, or cyclic hydrocarbon radical, or combination thereof, which
may be fully saturated, mono- or polyunsaturated and can include
di- and multivalent radicals, having the number of carbon atoms
designated (i.e. C.sub.1-C.sub.10 means one to ten carbons). In
some embodiments, the term "alkyl" means a straight or branched
chain, or combinations thereof, which may be fully saturated, mono-
or polyunsaturated and can include di- and multivalent radicals.
Examples of saturated hydrocarbon radicals include, but are not
limited to, groups such as methyl, ethyl, n-propyl, isopropyl,
n-butyl, t-butyl, isobutyl, sec-butyl, cyclohexyl,
(cyclohexyl)methyl, cyclopropylmethyl, homologs and isomers of, for
example, n-pentyl, n-hexyl, n-heptyl, n-octyl, and the like. An
unsaturated alkyl group is one having one or more double bonds or
triple bonds. Examples of unsaturated alkyl groups include, but are
not limited to, vinyl, 2-propenyl, crotyl, 2-isopentenyl,
2-(butadienyl), 2,4-pentadienyl, 3-(1,4-pentadienyl), ethynyl, 1-
and 3-propynyl, 3-butynyl, and the higher homologs and isomers.
[0020] The term "alkylene" by itself or as part of another
substituent means a divalent radical derived from an alkane, as
exemplified, but not limited, by
--CH.sub.2CH.sub.2CH.sub.2CH.sub.2--, and further includes those
groups described below as "heteroalkylene." Typically, an alkyl (or
alkylene) group will have from 1 to 24 carbon atoms, with those
groups having 10 or fewer carbon atoms being preferred in the
invention. A "lower alkyl" or "lower alkylene" is a shorter chain
alkyl or alkylene group, generally having eight or fewer carbon
atoms.
[0021] The term "alkenylene" by itself or as part of another
substituent means a divalent radical derived from an alkene.
[0022] The term "cycloalkylene" by itself or as part of another
substituent means a divalent radical derived from a
cycloalkane.
[0023] The term "heteroalkylene" by itself or as part of another
substituent means a divalent radical derived from an
heteroalkane.
[0024] The term "heterocycloalkylene" by itself or as part of
another substituent means a divalent radical derived from an
heterocycloalkane.
[0025] The term "arylene" by itself or as part of another
substituent means a divalent radical derived from an aryl.
[0026] The term "heteroarylene" by itself or as part of another
substituent means a divalent radical derived from heteroaryl.
[0027] The terms "alkoxy," "alkylamino" and "alkylthio" (or
thioalkoxy) are used in their conventional sense, and refer to
those alkyl groups attached to the remainder of the molecule via an
oxygen atom, an amino group, or a sulfur atom, respectively.
[0028] The term "heteroalkyl," by itself or in combination with
another term, means, unless otherwise stated, a stable straight or
branched chain, or cyclic hydrocarbon radical, or combinations
thereof, consisting of the stated number of carbon atoms and at
least one heteroatom. In some embodiments, the term "heteroalkyl,"
by itself or in combination with another term, means a stable
straight or branched chain, or combinations thereof, consisting of
the stated number of carbon atoms and at least one heteroatom. In
an exemplary embodiment, the heteroatoms can be selected from the
group consisting of B, O, N and S, and wherein the nitrogen and
sulfur atoms may optionally be oxidized and the nitrogen heteroatom
may optionally be quaternized. The heteroatom(s) B, O, N and S may
be placed at any interior position of the heteroalkyl group or at
the position at which the alkyl group is attached to the remainder
of the molecule. Examples include, but are not limited to,
--CH.sub.2--CH.sub.2--O--CH.sub.3,
--CH.sub.2--CH.sub.2--NH--CH.sub.3,
--CH.sub.2--CH.sub.2--N(CH.sub.3)--CH.sub.3,
--CH.sub.2--S--CH.sub.2--CH.sub.3, --CH.sub.2--CH.sub.2,
--S(O)--CH.sub.3, --CH.sub.2--CH.sub.2--S(O).sub.2--CH.sub.3,
--CH.dbd.CH--O--CH.sub.3, --CH.sub.2--CH.dbd.N--OCH.sub.3, and
--CH.dbd.CH--N(CH.sub.3)--CH.sub.3. Up to two heteroatoms may be
consecutive, such as, for example, --CH.sub.2--NH--OCH.sub.3.
Similarly, the term "heteroalkylene" by itself or as part of
another substituent means a divalent radical derived from
heteroalkyl, as exemplified, but not limited by,
--CH.sub.2--CH.sub.2--S--CH.sub.2--CH.sub.2-- and
--CH.sub.2--S--CH.sub.2--CH.sub.2--NH--CH.sub.2--. For
heteroalkylene groups, heteroatoms can also occupy either or both
of the chain termini (e.g., alkyleneoxy, alkylenedioxy,
alkyleneamino, alkylenediamino, and the like). Still further, for
alkylene and heteroalkylene linking groups, no orientation of the
linking group is implied by the direction in which the formula of
the linking group is written. For example, the formula
--C(O).sub.2R'-- represents both --C(O).sub.2R'- and
--R'C(O).sub.2--.
[0029] The terms "cycloalkyl" and "heterocycloalkyl", by themselves
or in combination with other terms, represent, unless otherwise
stated, cyclic versions of "alkyl" and "heteroalkyl", respectively.
Additionally, for heterocycloalkyl, a heteroatom can occupy the
position at which the heterocycle is attached to the remainder of
the molecule. Examples of cycloalkyl include, but are not limited
to, cyclopentyl, cyclohexyl, 1-cyclohexenyl, 3-cyclohexenyl,
cycloheptyl, and the like. Examples of heterocycloalkyl include,
but are not limited to, 1-(1,2,5,6-tetrahydropyridyl),
1-piperidinyl, 2-piperidinyl, 3-piperidinyl, 4-morpholinyl,
3-morpholinyl, tetrahydrofuran-2-yl, tetrahydrofuran-3-yl,
tetrahydrothien-2-yl, tetrahydrothien-3-yl, 1-piperazinyl,
2-piperazinyl, and the like.
[0030] The terms "halo" or "halogen," by themselves or as part of
another substituent, mean, unless otherwise stated, a fluorine,
chlorine, bromine, or iodine atom. Additionally, terms such as
"haloalkyl," are meant to include monohaloalkyl and polyhaloalkyl.
For example, the term "halo(C.sub.1-C.sub.4)alkyl" is mean to
include, but not be limited to, trifluoromethyl,
2,2,2-trifluoroethyl, 4-chlorobutyl, 3-bromopropyl, and the
like.
[0031] The term "aryl" means, unless otherwise stated, a
polyunsaturated, aromatic, substituent that can be a single ring or
multiple rings (preferably from 1 or 2 or 3 rings), which are fused
together or linked covalently. The term "heteroaryl" refers to aryl
groups (or rings) that contain from one to four heteroatoms. In an
exemplary embodiment, the heteroatom is selected from B, N, O, and
S, wherein the nitrogen and sulfur atoms are optionally oxidized,
and the nitrogen atom(s) are optionally quaternized. A heteroaryl
group can be attached to the remainder of the molecule through a
heteroatom. Non-limiting examples of aryl and heteroaryl groups
include phenyl, 1-naphthyl, 2-naphthyl, 4-biphenyl, 1-pyrrolyl,
2-pyrrolyl, 3-pyrrolyl, 3-pyrazolyl, 2-imidazolyl, 4-imidazolyl,
pyrazinyl, 2-oxazolyl, 4-oxazolyl, 2-phenyl-4-oxazolyl, 5-oxazolyl,
3-isoxazolyl, 4-isoxazolyl, 5-isoxazolyl, 2-thiazolyl, 4-thiazolyl,
5-thiazolyl, 2-furyl, 3-furyl, 2-thienyl, 3-thienyl, 2-pyridyl,
3-pyridyl, 4-pyridyl, 2-pyrimidyl, 4-pyrimidyl, 5-benzothiazolyl,
purinyl, 2-benzimidazolyl, 5-indolyl, 1-isoquinolyl, 5-isoquinolyl,
2-quinoxalinyl, 5-quinoxalinyl, 3-quinolyl, and 6-quinolyl.
Substituents for each of the above noted aryl and heteroaryl ring
systems are selected from the group of acceptable substituents
described below.
[0032] For brevity, the term "aryl" when used in combination with
other terms (e.g., aryloxy, arylthioxy, arylalkyl) includes both
aryl and heteroaryl rings as defined above. Thus, the term
"arylalkyl" is meant to include those radicals in which an aryl
group is attached to an alkyl group (e.g., benzyl, phenethyl,
pyridylmethyl and the like) including those alkyl groups in which a
carbon atom (e.g., a methylene group) has been replaced by, for
example, an oxygen atom (e.g., phenoxymethyl, 2-pyridyloxymethyl,
3-(1-naphthyloxy)propyl, and the like).
[0033] Each of the above terms (e.g., "alkyl," "heteroalkyl,"
"aryl" and "heteroaryl") are meant to include both substituted and
unsubstituted forms of the indicated radical. Preferred
substituents for each type of radical are provided below.
[0034] Substituents for the alkyl and heteroalkyl radicals
(including those groups often referred to as alkylene, alkenyl,
heteroalkylene, heteroalkenyl, alkynyl, cycloalkyl,
heterocycloalkyl, cycloalkenyl, and heterocycloalkenyl) are
generically referred to as "alkyl group substituents," and they can
be one or more of a variety of groups selected from, but not
limited to: --R', --OR', .dbd.O, .dbd.NR', .dbd.N--OR', --NR'R'',
--SR', -halogen, --SiR'R''R''', --OC(O)R', --C(O)R', --CO.sub.2R',
--CONR'R'', --OC(O)NR'R'', --NR''C(O)R', --NR'--C(O)NR''R''',
--NR''C(O).sub.2R', --NR'''''-C(NR'R''R''').dbd.NR'''',
--NR''''--C(NR'R'').dbd.NR', --S(O)R', --S(O).sub.2R',
--S(O).sub.2NR'R'', --NR''SO.sub.2R', --CN, --NO.sub.2, --N.sub.3,
--CH(Ph).sub.2, fluoro(C.sub.1-C.sub.4)alkoxy, and
fluoro(C.sub.1-C.sub.4)alkyl, in a number ranging from zero to
(2m'+1), where m' is the total number of carbon atoms in such
radical. R', R'', R''', R'''' and R''''' each preferably
independently refer to hydrogen, substituted or unsubstituted
heteroalkyl, substituted or unsubstituted aryl, e.g., aryl
substituted with 1-3 halogens, substituted or unsubstituted alkyl,
alkoxy or thioalkoxy groups, or arylalkyl groups. When a compound
of the invention includes more than one R group, for example, each
of the R groups is independently selected as are each R', R'',
R''', R'''' and R''''' groups when more than one of these groups is
present. When R' and R'' are attached to the same nitrogen atom,
they can be combined with the nitrogen atom to form a 5-, 6-, or
7-membered ring. For example, --NR'R'' is meant to include, but not
be limited to, 1-pyrrolidinyl and 4-morpholinyl. From the above
discussion of substituents, one of skill in the art will understand
that the term "alkyl" is meant to include groups including carbon
atoms bound to groups other than hydrogen groups, such as haloalkyl
(e.g., --CF.sub.3 and --CH.sub.2CF.sub.3) and acyl (e.g.,
--C(O)CH.sub.3, --C(O)CF.sub.3, --C(O)CH.sub.2OCH.sub.3, and the
like).
[0035] Similar to the substituents described for the alkyl radical,
substituents for the aryl and heteroaryl groups are generically
referred to as "aryl group substituents." The substituents are
selected from, for example: --R', --OR', .dbd.O, .dbd.NR',
.dbd.N--OR', --NR'R'', --SR', -halogen, --SiR'R''R''', --OC(O)R',
--C(O)R', --CO.sub.2R', --CONR'R'', --OC(O)NR'R'', --NR''C(O)R',
--NR'--C(O)NR''R''', --NR''C(O).sub.2R',
--NR'''''-C(NR'R''R''').dbd.NR'''', --NR''''--C(NR'R'').dbd.NR',
--S(O)R', --S(O).sub.2R', --S(O).sub.2NR'R'', --NR''SO.sub.2R',
--CN, --NO.sub.2, --N.sub.3, --CH(Ph).sub.2,
fluoro(C.sub.1-C.sub.4)alkoxy, and fluoro(C.sub.1-C.sub.4)alkyl, in
a number ranging from zero to the total number of open valences on
the aromatic ring system; and where R', R'', R''', R'''' and R'''''
are preferably independently selected from hydrogen, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted aryl and substituted or unsubstituted
heteroaryl. When a compound of the invention includes more than one
R group, for example, each of the R groups is independently
selected as are each R', R'', R''', R'''' and R''''' groups when
more than one of these groups is present.
[0036] Two of the substituents on adjacent atoms of the aryl or
heteroaryl ring may optionally be replaced with a substituent of
the formula -T-C(O)--(CRR').sub.q-U-, wherein T and U are
independently --NR--, --O--, --CRR'-- or a single bond, and q is an
integer of from 0 to 3. Alternatively, two of the substituents on
adjacent atoms of the aryl or heteroaryl ring may optionally be
replaced with a substituent of the formula
-A-(CH.sub.2).sub.r--B--, wherein A and B are independently
--CRR'--, --O--, --NR--, --S--, --S(O)--, --S(O).sub.2--,
--S(O).sub.2NR'-- or a single bond, and r is an integer of from 1
to 4. One of the single bonds of the new ring so formed may
optionally be replaced with a double bond. Alternatively, two of
the substituents on adjacent atoms of the aryl or heteroaryl ring
may optionally be replaced with a substituent of the formula
--(CRR').sub.s-X--(CR''R').sub.d--, where s and d are independently
integers of from 0 to 3, and X is --O--, --NR'--, --S--, --S(O)--,
--S(O).sub.2--, or --S(O).sub.2NR'--. The substituents R, R', R''
and R''' are preferably independently selected from hydrogen or
substituted or unsubstituted C.sub.1 or C.sub.2 or C.sub.3 or
C.sub.4 or C.sub.5 or C.sub.6 alkyl.
[0037] "Ring" as used herein, means a substituted or unsubstituted
cycloalkyl, substituted or unsubstituted heterocycloalkyl,
substituted or unsubstituted aryl, or substituted or unsubstituted
heteroaryl. A ring includes fused ring moieties. The number of
atoms in a ring is typically defined by the number of members in
the ring. For example, a "5- to 7-membered ring" means there are 5
or 6 or 7 atoms in the encircling arrangement. Unless otherwise
specified, the ring optionally includes a heteroatom. Thus, the
term "5- to 7-membered ring" includes, for example phenyl,
pyridinyl and piperidinyl. The term "5- to 7-membered
heterocycloalkyl ring", on the other hand, would include pyridinyl
and piperidinyl, but not phenyl. The term "ring" further includes a
ring system comprising more than one "ring", wherein each "ring" is
independently defined as above.
[0038] As used herein, the term "heteroatom" includes atoms other
than carbon (C) and hydrogen (H). Examples include oxygen (O),
nitrogen (N), sulfur (S), silicon (Si), germanium (Ge), aluminum
(Al) and boron (B).
[0039] The term "leaving group" means a functional group or atom
which can be dis placed by another functional group or atom in a
substitution reaction, such as a nucleophilic substitution
reaction. By way of example, representative leaving groups include
triflate, chloro, bromo and iodo groups; sulfonic ester groups,
such as mesylate, tosylate, brosylate, nosylate and the like; and
acyloxy groups, such as acetoxy, trifluoroacetoxy and the like.
[0040] The symbol "R" is a general abbreviation that represents a
substituent group that is selected from substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted aryl, substituted or unsubstituted
heteroaryl, substituted or unsubstituted cycloalkyl and substituted
or unsubstituted heterocycloalkyl groups.
[0041] By "effective" amount of a drug, formulation, or permeant is
meant a sufficient amount of an active agent to provide the desired
local or systemic effect. A "Topically effective,"
"pharmaceutically effective," or "therapeutically effective" amount
refers to the amount of drug needed to effect the desired
therapeutic result.
[0042] "Topically effective" refers to a material that, when
applied to the skin, nail, hair, claw or hoof produces a desired
pharmacological result either locally at the place of application
or systemically as a result of transdermal passage of an active
ingredient in the material.
[0043] The term "pharmaceutically acceptable salt" is meant to
include a salt of a compound of the invention which is prepared
with relatively nontoxic acids or bases, depending on the
particular substituents found on the compounds described herein.
When compounds of the invention contain relatively acidic
functionalities, base addition salts can be obtained by contacting
the neutral form of such compounds with a sufficient amount of the
desired base, either neat or in a suitable inert solvent. Examples
of pharmaceutically acceptable base addition salts include sodium,
potassium, calcium, ammonium, organic amino (such as choline or
diethylamine or amino acids such as d-arginine, l-arginine,
d-lysine, l-lysine), or magnesium salt, or a similar salt. When
compounds of the invention contain relatively basic
functionalities, acid addition salts can be obtained by contacting
the neutral form of such compounds with a sufficient amount of the
desired acid, either neat or in a suitable inert solvent. Examples
of pharmaceutically acceptable acid addition salts include those
derived from inorganic acids like hydrochloric, hydrobromic,
nitric, carbonic, monohydrogencarbonic, phosphoric,
monohydrogenphosphoric, dihydrogenphosphoric, sulfuric,
monohydrogensulfuric, hydriodic, or phosphorous acids and the like,
as well as the salts derived from relatively nontoxic organic acids
like acetic, propionic, isobutyric, maleic, malonic, benzoic,
succinic, suberic, fumaric, lactic, mandelic, phthalic,
benzenesulfonic, p-tolylsulfonic, citric, tartaric,
methanesulfonic, and the like. Also included are salts of amino
acids such as arginate and the like, and salts of organic acids
like glucuronic or galactunoric acids and the like (see, for
example, Berge et al., "Pharmaceutical Salts", Journal of
Pharmaceutical Science 66: 1-19 (1977)). Certain specific compounds
of the invention contain both basic and acidic functionalities that
allow the compounds to be converted into either base or acid
addition salts.
[0044] The neutral forms of the compounds are preferably
regenerated by contacting the salt with a base or acid and
isolating the parent compounds in the conventional manner. The
parent form of the compound differs from the various salt forms in
certain physical properties, such as solubility in polar
solvents.
[0045] In addition to salt forms, the invention provides compounds
which are in a prodrug form. Prodrugs of the compounds described
herein readily undergo chemical changes under physiological
conditions to provide the compounds of the invention. Additionally,
prodrugs can be converted to the compounds of the invention by
chemical or biochemical methods in an ex vivo environment.
[0046] Certain compounds of the invention can exist in unsolvated
forms as well as solvated forms, including hydrated forms. In
general, the solvated forms are equivalent to unsolvated forms and
are encompassed within the scope of the invention. Certain
compounds of the invention may exist in multiple crystalline or
amorphous forms.
[0047] Certain compounds of the invention possess asymmetric carbon
atoms (optical centers) or double bonds; the racemates,
diastereomers, geometric isomers and individual isomers are
encompassed within the scope of the invention. The graphic
representations of racemic, ambiscalemic and scalemic or
enantiomerically pure compounds used herein are taken from Maehr,
J. Chem. Ed. 1985, 62: 114-120. Solid and broken wedges are used to
denote the absolute configuration of a stereocenter unless
otherwise noted. When the compounds described herein contain
olefinic double bonds or other centers of geometric asymmetry, and
unless specified otherwise, it is intended that the compounds
include both E and Z geometric isomers. Likewise, all tautomeric
forms are included.
[0048] Compounds of the invention can exist in particular geometric
or stereoisomeric forms. The invention contemplates all such
compounds, including cis- and trans-isomers, (-)- and
(+)-enantiomers, (R)- and (S)-enantiomers, diastereomers,
(D)-isomers, (L)-isomers, the racemic mixtures thereof, and other
mixtures thereof, such as enantiomerically or diastereomerically
enriched mixtures, as falling within the scope of the invention.
Additional asymmetric carbon atoms can be present in a substituent
such as an alkyl group. All such isomers, as well as mixtures
thereof, are intended to be included in this invention.
[0049] Optically active (R)- and (S)-isomers and d and l isomers
can be prepared using chiral synthons or chiral reagents, or
resolved using conventional techniques. If, for instance, a
particular enantiomer of a compound of the invention is desired, it
can be prepared by asymmetric synthesis, or by derivatization with
a chiral auxiliary, where the resulting diastereomeric mixture is
separated and the auxiliary group cleaved to provide the pure
desired enantiomers. Alternatively, where the molecule contains a
basic functional group, such as an amino group, or an acidic
functional group, such as a carboxyl group, diastereomeric salts
can be formed with an appropriate optically active acid or base,
followed by resolution of the diastereomers thus formed by
fractional crystallization or chromatographic means known in the
art, and subsequent recovery of the pure enantiomers. In addition,
separation of enantiomers and diastereomers is frequently
accomplished using chromatography employing chiral, stationary
phases, optionally in combination with chemical derivatization
(e.g., formation of carbamates from amines).
[0050] The compounds of the invention may also contain unnatural
proportions of atomic isotopes at one or more of the atoms that
constitute such compounds. For example, the compounds may be
radiolabeled with radioactive isotopes, such as for example tritium
(.sup.3H), iodine-125 (.sup.125I) or carbon-14 (.sup.14C). The
compounds may also be labeled with stable isotopes such as
deuterium. All isotopic variations of the compounds of the
invention, whether radioactive or not, are intended to be
encompassed within the scope of the invention.
[0051] The term "pharmaceutically acceptable carrier" or
"pharmaceutically acceptable vehicle" refers to any formulation or
carrier medium that provides the appropriate delivery of an
effective amount of an active agent as defined herein, does not
interfere with the effectiveness of the biological activity of the
active agent, and that is sufficiently non-toxic to the animal.
Representative carriers include water, oils, both vegetable and
mineral, cream bases, lotion bases, ointment bases and the like.
These bases include suspending agents, thickeners, penetration
enhancers, and the like. Their formulation is well known to those
in the pharmaceutical arts. Additional information concerning
carriers can be found in Remington: The Science and Practice of
Pharmacy, 21st Ed., Lippincott, Williams & Wilkins (2005) which
is incorporated herein by reference.
[0052] The term "pharmaceutically acceptable additive" refers to
preservatives, antioxidants, fragrances, emulsifiers, dyes and
excipients known or used in the field of drug formulation and that
do not unduly interfere with the effectiveness of the biological
activity of the active agent, and that is sufficiently non-toxic to
the animal. Additives for topical formulations are well-known in
the art, and may be added to the topical composition, as long as
they are pharmaceutically acceptable and not deleterious to the
epithelial cells or their function. Further, they should not cause
deterioration in the stability of the composition. For example,
inert fillers, anti-irritants, tackifiers, excipients, fragrances,
opacifiers, antioxidants, gelling agents, stabilizers, surfactant,
emollients, coloring agents, preservatives, buffering agents, other
permeation enhancers, and other conventional components of topical
or transdermal delivery formulations as are known in the art.
[0053] The term "excipients" is conventionally known to mean
carriers, diluents, vehicles, and or additives used in formulating
drug compositions effective for the desired use.
[0054] The terms "effective amount" or a "therapeutically effective
amount" of a drug or pharmacologically active agent refers to a
nontoxic but sufficient amount of the drug or agent to provide the
desired effect. In the oral dosage forms of the present disclosure,
an "effective amount" of one active of the combination is the
amount of that active that is effective to provide the desired
effect when used in combination with the other active of the
combination. The amount that is "effective" will vary from subject
to subject, depending on the age and general condition of the
individual, the particular active agent or agents, and the
appropriate "effective" amount in any individual case may be
determined by one of ordinary skill in the art using routine
experimentation.
[0055] The phrases "active ingredient", "therapeutic agent",
"active", or "active agent" mean a chemical entity which can be
effective in treating a targeted disorder, disease or
condition.
[0056] The phrase "pharmaceutically acceptable" means moieties or
compounds that are, within the scope of medical judgment, suitable
for use in humans without causing undesirable biological effects
such as undue toxicity, irritation, allergic response, and the
like, for example.
[0057] The phrase "unit", as used herein, refers to the number of
discrete objects to be administered which comprise the dosage form.
In some embodiments, the dosage form includes a compound of the
invention in one capsule. This is a single unit. In some
embodiments, the dosage form includes a compound of the invention
as part of a therapeutically effective dosage of a cream or
ointment. This is also a single unit. In some embodiments, the
dosage form includes a compound of the invention and another active
ingredient contained within one capsule, or as part of a
therapeutically effective dosage of a topical formulation, such as
a cream or an ointment, for example. This is a single unit, whether
or not the interior of the capsule includes multiple discrete
granules of the active ingredient. In some embodiments, the dosage
form includes a compound of the invention in one capsule, and the
active ingredient in a second capsule. This is a two unit dosage
form, such as two capsules or tablets, and so such units are
contained in a single package. Thus the term `unit` refers to the
object which is administered to the animal, not to the interior
components of the object.
[0058] The term, "prodrug", as defined herein, is a derivative of a
parent drug molecule that exerts its pharmacological effect only
after chemical and/or enzymatic conversion to its active form in
vivo. Prodrugs include those designed to circumvent problems
associated with delivery of the parent drug. This may be due to
poor physicochemical properties, such as poor chemical stability or
low aqueous solubility, and may also be due to poor pharmacokinetic
properties, such as poor bioavailability or poor half-life. Thus,
certain advantages of prodrugs may include improved chemical
stability, absorption, and/or PK properties of the parent
carboxylic acids. Prodrugs may also be used to make drugs more
amenable to the animal, by minimizing the frequency (e.g., once
daily) or route of dosing (e.g., oral), or to improve the taste or
odor if given orally, or to minimize pain if given
parenterally.
[0059] "Biological medium," as used herein refers to both in vitro
and in vivo biological milieus. Exemplary in vitro "biological
media" include, but are not limited to, cell culture, tissue
culture, homogenates, plasma and blood. In vivo applications are
generally performed in mammals, preferably humans.
[0060] "Inhibiting" and "blocking," are used interchangeably herein
to refer to the partial or full blockade of an enzyme, such as a
beta-lactamase or a leucyl t-RNA synthetase or a
phosphodiesterase.
[0061] Boron is able to form additional covalent or dative bonds
with oxygen, sulfur or nitrogen under some circumstances in this
invention.
[0062] Embodiments of the invention also encompass compounds that
are poly- or multi-valent species, including, for example, species
such as dimers, trimers, tetramers and higher homologs of the
compounds of use in the invention or reactive analogues
thereof.
[0063] "Salt counterion", as used herein, refers to positively
charged ions that associate with a compound of the invention when
the boron is fully negatively or partially negatively charged.
Examples of salt counterions include H.sup.+, H.sub.3O.sup.+,
ammonium, potassium, calcium, magnesium, organic amino (such as
choline or diethylamine or amino acids such as d-arginine,
l-arginine, d-lysine, l-lysine), and sodium.
[0064] The compounds comprising a boron bonded to a carbon and
three heteroatoms (such as three oxygens described in this section)
can optionally contain a fully negatively charged boron or
partially negatively charged boron. Due to the negative charge, a
positively charged counterion may associate with this compound,
thus forming a salt. Examples of positively charged counterions
include H.sup.+, H.sub.3O.sup.+, ammonium, potassium, calcium,
magnesium, organic amino (such as choline or diethylamine or amino
acids such as d-arginine, l-arginine, d-lysine, l-lysine), and
sodium. These salts of the compounds are implicitly contained in
descriptions of these compounds.
II. Introduction
[0065] The invention provides novel boron compounds and methods for
the preparation of these molecules. The invention further provides
methods of treating bacterial infections, killing and/or inhibiting
the growth of bacteria in part or wholly through the use of the
compounds described herein. In another aspect, the invention is a
combination of a compound of the invention and an antibacterial. In
another aspect, the invention is a pharmaceutical formulation
comprising a pharmaceutically acceptable excipient and a compound
of the invention. In another aspect, the invention is a
pharmaceutical formulation comprising a compound of the invention,
an antibacterial, and a pharmaceutically acceptable excipient.
III. a) Compounds
[0066] In one aspect the invention provides a compound of the
invention. In an exemplary embodiment, the invention provides a
compound described herein, or a salt or a hydrate or a solvate
thereof. In an exemplary embodiment, the salt of a compound
described herein is a pharmaceutically acceptable salt. In an
exemplary embodiment, the invention provides a compound described
herein, or a pharmaceutically acceptable salt thereof. In an
exemplary embodiment, the invention provides a compound described
in a formula provided herein. In an exemplary embodiment, the
invention provides a compound described herein.
[0067] In an exemplary embodiment, the compound has a structure
which is
##STR00003##
wherein W is H or a bond to X; X is
##STR00004##
wherein R.sup.a and R.sup.b are each independently selected from
the group consisting of R.sup.15, --OR.sup.15, --NR.sup.15R.sup.16,
--SR.sup.15, --S(O)R.sup.15, --S(O).sub.2R.sup.15,
--S(O).sub.2NR.sup.15R.sup.16, --C(O)R.sup.15, --C(O)OR.sup.15, and
--C(O)NR.sup.15R.sup.16 wherein R.sup.15 and R.sup.16 are each
independently selected from the group consisting of H, halogen,
cyano, nitro, --OR.sup.17, --NR.sup.17R.sup.18, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl, wherein R.sup.17 and
R.sup.18 are each independently selected from the group consisting
of H, substituted or unsubstituted alkyl, substituted or
unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl,
substituted or unsubstituted heterocycloalkyl, substituted or
unsubstituted aryl, and substituted or unsubstituted heteroaryl,
and wherein R.sup.15 and R.sup.16, and/or R.sup.17 and R.sup.18,
along with the nitrogen to which they are connected, are optionally
joined to form a substituted or unsubstituted 4- to 8-membered
ring, with the proviso that R.sup.a and R.sup.b are not both H; or
X is
##STR00005##
wherein R.sup.c is --OR.sup.15, --NR.sup.15R.sup.16, --SR.sup.15,
--S(O)R.sup.15, --S(O).sub.2R.sup.15, --S(O).sub.2N.sup.15R.sup.16,
--C(O)R.sup.15, --C(O)OR.sup.15, and --C(O)N.sup.15R.sup.16,
wherein R.sup.15 and R.sup.16 are each independently selected from
the group consisting of H, halogen, cyano, nitro, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl, and wherein R.sup.15
and R.sup.16, along with the nitrogen to which they are connected,
are optionally joined to form a substituted or unsubstituted 4- to
8-membered ring, or X is
##STR00006##
or X is
##STR00007##
[0068] wherein R.sup.d and R.sup.e are each independently selected
from the group consisting of H, halogen, cyano, nitro, substituted
or unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl, --OR.sup.15,
--NR.sup.15R.sup.16, --SR.sup.15, --S(O)R.sup.15,
--S(O).sub.2R.sup.15, --S(O).sub.2NR.sup.15R.sup.16,
--C(O)R.sup.15, --C(O)OR.sup.15, and --C(O)NR.sup.15R.sup.16,
wherein R.sup.15 and R.sup.16 are each independently selected from
the group consisting of H, halogen, cyano, nitro, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl, and wherein R.sup.d
and R.sup.e, along with the atom to which they are connected, are
optionally joined to form a substituted or unsubstituted 3- to
8-membered ring, and wherein R.sup.15 and R.sup.16, along with the
nitrogen to which they are connected, are optionally joined to form
a substituted or unsubstituted 4- to 8-membered ring with the
proviso that R.sup.d and R.sup.e are not both H, wherein X
optionally comprises an attachment point to W; Y is selected from
the group consisting of a bond, --O--, --S--, --NH--, substituted
or unsubstituted alkylene, and substituted or unsubstituted
heteroalkylene; and Z is a substituted or unsubstituted
heterocyclic ring or ring system containing at least one endocyclic
boron.
[0069] In an exemplary embodiment, the compound is Formula (I), W,
Y and Z are as described herein, and X is
##STR00008##
wherein R.sup.15 is selected from the group consisting of H,
substituted or unsubstituted alkyl, substituted or unsubstituted
heteroalkyl, substituted or unsubstituted cycloalkyl, substituted
or unsubstituted heterocycloalkyl, substituted or unsubstituted
aryl, and substituted or unsubstituted heteroaryl. In an exemplary
embodiment, Y and Z are as described herein, and X is
##STR00009##
wherein R.sup.15 and R.sup.16 are each independently selected from
the group consisting of H, --OR.sup.17, --NR.sup.17R.sup.18,
substituted or unsubstituted alkyl, substituted or unsubstituted
heteroalkyl, substituted or unsubstituted cycloalkyl, substituted
or unsubstituted heterocycloalkyl, substituted or unsubstituted
aryl, and substituted or unsubstituted heteroaryl, wherein R.sup.17
and R.sup.18 are each independently selected from the group
consisting of H, substituted or unsubstituted alkyl, substituted or
unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl,
substituted or unsubstituted heterocycloalkyl, substituted or
unsubstituted aryl, and substituted or unsubstituted heteroaryl,
and wherein R.sup.15 and R.sup.16, and/or R.sup.17 and R.sup.18,
along with the nitrogen to which they are connected, are optionally
joined to form a substituted or unsubstituted 4- to 8-membered
ring. In an exemplary embodiment, the compound is Formula (I), W, Y
and Z are as described herein, and X is
##STR00010##
wherein R.sup.c is selected from the group consisting of H,
substituted or unsubstituted alkyl, and --OR.sup.15 wherein
R.sup.15 is H or substituted or unsubstituted alkyl. In an
exemplary embodiment, the compound is Formula (I), W, Y and Z are
as described herein, and X is
##STR00011##
wherein R.sup.d is selected from the group consisting of halogen,
substituted or unsubstituted alkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, --OR.sup.15,
--SR.sup.15, --S(O)R.sup.15, --NR.sup.15R.sup.16, --C(O)R.sup.15,
--CH.sub.2C(O)OR.sup.15, and --CH.sub.2C(O)NR.sup.15R.sup.16,
wherein R.sup.15 and R.sup.16 are each independently selected from
the group consisting of H, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, and
substituted or unsubstituted heteroaryl, and wherein R.sup.15 and
R.sup.16, along with the nitrogen to which they are connected, are
optionally joined to form a substituted or unsubstituted 4- to
8-membered ring.
[0070] In an exemplary embodiment, the compound is Formula (I), W,
Y and Z are as described herein, and X is
##STR00012##
[0071] In an exemplary embodiment, the compound is Formula (I), W,
X and Z are as described herein, and Y is substituted alkylene. In
an exemplary embodiment, the compound is Formula (I), W, X and Z
are as described herein, and Y is unsubstituted alkylene. In an
exemplary embodiment, the compound is Formula (I), W, X and Z are
as described herein, and Y is methylene. In an exemplary
embodiment, the compound is Formula (I), W, X and Z are as
described herein, and Y is ethylene. In an exemplary embodiment,
the compound is Formula (I), W, X and Z are as described herein,
and Y is propylene. In an exemplary embodiment, the compound is
Formula (I), W, X and Z are as described herein, and Y is
substituted heteroalkylene. In an exemplary embodiment, the
compound is Formula (I), W, X and Z are as described herein, and Y
is unsubstituted heteroalkylene. In an exemplary embodiment, the
compound is Formula (I), W, X and Z are as described herein, and Y
is *--OCH.sub.2--. In an exemplary embodiment, the compound is
Formula (I), W, X and Z are as described herein, and Y is
*--SCH.sub.2--. In an exemplary embodiment, the compound is Formula
(I), W, X and Z are as described herein, and Y is *--NHCH.sub.2--.
In an exemplary embodiment, the compound is Formula (I), W, X and Z
are as described herein, and Y is *--CH.sub.2NH--. In an exemplary
embodiment, the compound is Formula (I), W, X and Z are as
described herein, and Y is *--C(O)NH--. In an exemplary embodiment,
the compound is Formula (I), W, X and Z are as described herein,
and Y is *--CH.sub.2NHCH.sub.2-- or 1-piperazinyl or
*--S(O)CH.sub.2-- or *--S(O).sub.2--. In an exemplary embodiment,
the compound is Formula (I), W, X and Z are as described herein,
and Y is 1-piperazinyl. In an exemplary embodiment, the compound is
Formula (I), W, X and Z are as described herein, and Y is
*--S(O)CH.sub.2--. In an exemplary embodiment, the compound is
Formula (I), W, X and Z are as described herein, and Y is
*--S(O).sub.2--. In an exemplary embodiment, the compound is
Formula (I), W, X and Z are as described herein, and Y is
*--S(O).sub.2CH.sub.2--. In an exemplary embodiment, the compound
is Formula (I), W, X and Z are as described herein, and Y is
*--NHC(O)OCH.sub.2--. In this paragraph, * represents the point of
attachment to Z.
[0072] In an exemplary embodiment, the compound is Formula (I), W,
X and Y are as described herein, and Z is substituted or
unsubstituted heteroaryl, wherein said heteroaryl comprises an
endocyclic boron. In an exemplary embodiment, the compound is
Formula (I), W, X and Y are as described herein, and Z is
substituted or unsubstituted heteroaryl, wherein said heteroaryl
has one ring, and said ring comprises an endocyclic boron. In an
exemplary embodiment, the compound is Formula (I), W, X and Y are
as described herein, and Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl has two rings, and one of the
two rings comprises an endocyclic boron.
[0073] In an exemplary embodiment, the compound is Formula (I), W,
X and Y are as described herein, and Z is substituted or
unsubstituted heterocycloalkyl, wherein said heterocycloalkyl
comprises an endocyclic boron. In an exemplary embodiment, the
compound is Formula (I), W, X and Y are as described herein, and Z
is substituted or unsubstituted heterocycloalkyl, wherein said
heterocycloalkyl has one ring, and said ring comprises an
endocyclic boron. In an exemplary embodiment, the compound is
Formula (I), W, X and Y are as described herein, and Z is
substituted or unsubstituted heterocycloalkyl, wherein said
heterocycloalkyl has two rings, and one of the two rings comprises
an endocyclic boron.
[0074] In an exemplary embodiment, the compound is Formula (I), W,
X and Y are as described herein, and Z is substituted or
unsubstituted benzoxaborole. In an exemplary embodiment, the
compound is Formula (I), W, X and Y are as described herein, and Z
is substituted or unsubstituted pyridinyloxaborole. In an exemplary
embodiment, the compound is Formula (I), W, X and Y are as
described herein, and Z is substituted or unsubstituted
benzoxaborininol. In an exemplary embodiment, the compound is
Formula (I), W, X and Y are as described herein, and Z is
substituted or unsubstituted benzoxazaborininol. In an exemplary
embodiment, the compound is Formula (I), W, X and Y are as
described herein, and Z is substituted or unsubstituted
benzodiazaborininol. In an exemplary embodiment, the compound is
Formula (I), W, X and Y are as described herein, and Z is
substituted or unsubstituted oxaborole. In an exemplary embodiment,
X the compound is Formula (I), and W and Y are as described herein,
and Z is substituted or unsubstituted dihydrobenzoazaborinine.
[0075] In an exemplary embodiment, the compound is Formula (I), W,
X and Y are as described herein, and said Z is
##STR00013##
wherein R.sup.3, R.sup.3a, R.sup.4, R.sup.5, and R.sup.7 are each
independently selected from the group consisting of R.sup.10,
--OR.sup.10, --NR.sup.10OR.sup.11, --SR.sup.10, --S(O)R.sup.10,
--S(O).sub.2R.sup.10, --S(O).sub.2NR.sup.10R.sup.11,
--C(O)R.sup.10, --C(O)OR.sup.10, and --C(O)NR.sup.10R.sup.11
wherein R.sup.10 and R.sup.11 are each independently selected from
the group consisting of H, halogen, cyano, nitro, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl.
[0076] In an exemplary embodiment, the compound is Formula (I), W,
X and Y are as described herein, and said Z is
##STR00014##
wherein R.sup.3, R.sup.3a, R.sup.4, R.sup.6, and R.sup.7 are each
independently selected from the group consisting of R.sup.1,
--OR.sup.10, --NR.sup.10R.sup.11, --SR.sup.10, --S(O)R.sup.10,
--S(O).sub.2R.sup.10, --S(O).sub.2NR.sup.10R.sup.11,
--C(O)R.sup.10, --C(O)OR.sup.10, and --C(O)NR.sup.10R.sup.11
wherein R.sup.10 and R.sup.11 are each independently selected from
the group consisting of H, halogen, cyano, nitro, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl.
[0077] In an exemplary embodiment, the compound is Formula (I), W,
X and Y are as described herein, and said Z is
##STR00015##
wherein R.sup.4, R.sup.5, and R.sup.7 are each independently
selected from the group consisting of R.sup.10, --OR.sup.10,
--NR.sup.10R.sup.11, wherein R.sup.10 and R.sup.11 are each
independently selected from the group consisting of H, halogen,
cyano, nitro, substituted or unsubstituted alkyl, and substituted
or unsubstituted heteroalkyl. In an exemplary embodiment, the
compound is Formula (I), W, X and Y are as described herein, and
said Z is
##STR00016##
In an exemplary embodiment, the compound is
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-7-(hydroxymethyl)-4,7,9,12-tetrame-
thyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hy-
droxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate. In an
exemplary embodiment, the compound is
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-((R)-oxiran-
-2-yl)-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1--
hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate. In an
exemplary embodiment, the compound is
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-((E)-2-(3-m-
ethyl-1,2,4-oxadiazol-5-yl)vinyl)-3-oxodecahydro-4,9a-propanocyclopenta[8]-
annulen-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)o-
xy)acetate.
[0078] In an exemplary embodiment, the compound is Formula (I), W,
Y and Z are as described herein, and said X is
##STR00017##
wherein R.sup.a and R.sup.b are each independently selected from
the group consisting of R.sup.15, --OR.sup.15, --NR.sup.15R.sup.16,
--SR.sup.15, --S(O)R.sup.15, --S(O).sub.2R.sup.15,
--S(O).sub.2NR.sup.15R.sup.16, --C(O)R.sup.15, --C(O)OR.sup.15, and
--C(O)NR.sup.15R.sup.16 wherein R.sup.15 and R.sup.16 are each
independently selected from the group consisting of H, halogen,
cyano, nitro, --OR.sup.17, --NR.sup.17R.sup.18, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl, wherein R.sup.17 and
R.sup.18 are each independently selected from the group consisting
of H, substituted or unsubstituted alkyl, substituted or
unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl,
substituted or unsubstituted heterocycloalkyl, substituted or
unsubstituted aryl, and substituted or unsubstituted heteroaryl,
and wherein R.sup.15 and R.sup.16, and/or R.sup.17 and R.sup.18,
along with the nitrogen to which they are connected, are optionally
joined to form a substituted or unsubstituted 4- to 8-membered
ring, with the proviso that R.sup.a and R.sup.b are not both H. In
an exemplary embodiment, the compound is Formula (I), W, Y and Z
are as described herein, and said X is
##STR00018##
wherein one of R.sup.a and R.sup.b is H, and the other of R.sup.a
and R.sup.b is selected from the group consisting of R.sup.15,
--OR.sup.15, --NR.sup.15R.sup.16, --SR.sup.15, --S(O)R.sup.15,
--S(O).sub.2R.sup.15, --S(O).sub.2N.sup.15R.sup.16, --C(O)R.sup.15,
--C(O)OR.sup.15, and --C(O)NR.sup.15R.sup.16 wherein R.sup.15 and
R.sup.16 are each independently selected from the group consisting
of H, halogen, cyano, nitro, --OR.sup.17, --NR.sup.17R.sup.18,
substituted or unsubstituted alkyl, substituted or unsubstituted
heteroalkyl, substituted or unsubstituted cycloalkyl, substituted
or unsubstituted heterocycloalkyl, substituted or unsubstituted
aryl, and substituted or unsubstituted heteroaryl, wherein R.sup.17
and R.sup.18 are each independently selected from the group
consisting of H, substituted or unsubstituted alkyl, substituted or
unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl,
substituted or unsubstituted heterocycloalkyl, substituted or
unsubstituted aryl, and substituted or unsubstituted heteroaryl,
and wherein R.sup.15 and R.sup.16, and/or R.sup.17 and R.sup.18,
along with the nitrogen to which they are connected, are optionally
joined to form a substituted or unsubstituted 4- to 8-membered
ring. In an exemplary embodiment, the compound is Formula (I), W, Y
and Z are as described herein, and said X is
##STR00019##
wherein one of R.sup.a and R.sup.b is H, and the other of R.sup.a
and R.sup.b is substituted or unsubstituted heteroaryl. In an
exemplary embodiment, the compound is Formula (I), W, Y and Z are
as described herein, and said X is
##STR00020##
wherein one of R.sup.a and R.sup.b is H, and the other of R.sup.a
and R.sup.b is unsubstituted oxadiazolyl. In an exemplary
embodiment, the compound is Formula (I), W, Y and Z are as
described herein, and said X is
##STR00021##
wherein one of R.sup.a and R.sup.b is H, and the other of R.sup.a
and R.sup.b is 1,2,4-oxadiazolyl. In an exemplary embodiment, the
compound is Formula (I), W, Y and Z are as described herein, and
said X is
##STR00022##
wherein one of R.sup.a and R.sup.b is H, and the other of R.sup.a
and R.sup.b is 1,2,4-oxadiazol-5-yl. In an exemplary embodiment,
the compound is Formula (I), W, Y and Z are as described herein,
and said X is
##STR00023##
wherein one of R.sup.a and R.sup.b is H, and the other of R.sup.a
and R.sup.b is substituted oxadiazolyl. In an exemplary embodiment,
the compound is Formula (I), W, Y and Z are as described herein,
and said X is
##STR00024##
wherein one of R.sup.a and R.sup.b is H, and the other of R.sup.a
and R.sup.b is oxadiazolyl, substituted with unsubstituted
C.sub.1-C.sub.6 alkyl.
[0079] In an exemplary embodiment, the compound is Formula (I), W,
Y and Z are as described herein, and said X is
##STR00025##
wherein one of R.sup.a and R.sup.b is H, and the other of R.sup.a
and R.sup.b is oxadiazolyl, substituted with unsubstituted
C.sub.1-C.sub.3 alkyl. In an exemplary embodiment, the compound is
Formula (I), W, Y and Z are as described herein, and said X is
##STR00026##
wherein one of R.sup.a and R.sup.b is H, and the other of R.sup.a
and R.sup.b is oxadiazolyl, substituted with methyl. In an
exemplary embodiment, the compound is Formula (I), W, Y and Z are
as described herein, and said X is
##STR00027##
wherein one of R.sup.a and R.sup.b is H, and the other of R.sup.a
and R.sup.b is 3-methyl 1,2,4-oxadiazol-5-yl.
[0080] In an exemplary embodiment, the compound is Formula (I), W,
Y and Z are as described herein, and said X is
##STR00028##
[0081] In an exemplary embodiment, the compound is Formula (I), W,
Y and Z are as described herein, and X is
##STR00029##
wherein R.sup.15 is selected from the group consisting of H,
substituted or unsubstituted alkyl, substituted or unsubstituted
heteroalkyl, substituted or unsubstituted cycloalkyl, substituted
or unsubstituted heterocycloalkyl, substituted or unsubstituted
aryl, and substituted or unsubstituted heteroaryl. In an exemplary
embodiment, the compound is Formula (I), W, Y and Z are as
described herein, and X is
##STR00030##
wherein R.sup.15 is H. In an exemplary embodiment, the compound is
Formula (I), W, Y and Z are as described herein, and X is
##STR00031##
wherein R.sup.15 is substituted alkyl. In an exemplary embodiment,
the compound is Formula (I), W, Y and Z are as described herein,
and X is
##STR00032##
wherein R.sup.15 is unsubstituted C.sub.1-C.sub.6 alkyl. In an
exemplary embodiment, the compound is Formula (I), W, Y and Z are
as described herein, and X is
##STR00033##
wherein R.sup.15 is unsubstituted C.sub.2-C.sub.4 alkyl. In an
exemplary embodiment, the compound is Formula (I), W, Y and Z are
as described herein, and X is
##STR00034##
wherein R.sup.15 is methyl.
[0082] In an exemplary embodiment, the compound is Formula (I), W,
Y and Z are as described herein, and X is
##STR00035##
wherein R.sup.d and R.sup.e are each independently selected from
the group consisting of H, halogen, cyano, nitro, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl, --OR.sup.15,
--NR.sup.15R.sup.16, --SR.sup.15, --S(O)R.sup.15,
--S(O).sub.2R.sup.15, --S(O).sub.2N.sup.15R.sup.16, --C(O)R.sup.15,
--C(O)OR.sup.15, and --C(O)N.sup.15R.sup.16, wherein R.sup.15 and
R.sup.16 are each independently selected from the group consisting
of H, halogen, cyano, nitro, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, and
substituted or unsubstituted heteroaryl, and wherein R.sup.d and
R.sup.e, along with the atom to which they are connected, are
optionally joined to form a substituted or unsubstituted 3- to
8-membered ring, and wherein R.sup.15 and R.sup.16, along with the
nitrogen to which they are connected, are optionally joined to form
a substituted or unsubstituted 4- to 8-membered ring with the
proviso that R.sup.d and R.sup.e are not both H. In an exemplary
embodiment, the compound is Formula (I), W, Y and Z are as
described herein, and X is
##STR00036##
wherein R.sup.d and R.sup.e are each independently selected from
C.sub.1-C.sub.3 alkyl.
[0083] In an exemplary embodiment, the compound is Formula (I), W,
Y and Z are as described herein, and X is
##STR00037##
wherein R.sup.d is selected from the group consisting of halogen,
substituted or unsubstituted alkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, --OR.sup.15,
--SR.sup.15, --S(O)R.sup.15, --NR.sup.15R.sup.16, --C(O)R.sup.15,
--CH.sub.2C(O)OR.sup.15, and --CH.sub.2C(O)N.sup.15R.sup.16,
wherein R.sup.15 and R.sup.16 are each independently selected from
the group consisting of H, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, and
substituted or unsubstituted heteroaryl, and wherein R.sup.15 and
R.sup.16, along with the nitrogen to which they are connected, are
optionally joined to form a substituted or unsubstituted 4- to
8-membered ring.
[0084] In an exemplary embodiment, the compound is Formula (I), W,
Y and Z are as described herein, and said X is
##STR00038##
wherein R.sup.d is OH. In an exemplary embodiment, the compound is
Formula (I), W, Y and Z are as described herein, and said X is
##STR00039##
wherein R.sup.d is --OR.sup.15, wherein R.sup.15 is substituted or
unsubstituted alkyl. In an exemplary embodiment, the compound is
Formula (I), W, Y and Z are as described herein, and said X is
##STR00040##
wherein R.sup.d is --OR.sup.15, wherein R.sup.15 is unsubstituted
C.sub.1-C.sub.6 alkyl. In an exemplary embodiment, the compound is
Formula (I), W, Y and Z are as described herein, and said X is
##STR00041##
wherein R.sup.d is --OR.sup.15, wherein R.sup.15 is methyl. In an
exemplary embodiment, the compound is Formula (I), W, Y and Z are
as described herein, and said X is
##STR00042##
wherein R.sup.d is --OR.sup.15, wherein R.sup.15 is ethyl or propyl
or isopropyl. In an exemplary embodiment, the compound is Formula
(I), W, Y and Z are as described herein, and said X is
C.sub.1-C.sub.6 alkyl substituted with at least one hydroxy. In an
exemplary embodiment, the compound is Formula (I), W, Y and Z are
as described herein, and said X is C.sub.3 alkyl substituted with
at least one hydroxy. In an exemplary embodiment, the compound is
Formula (I), W, Y and Z are as described herein, and said X is
ethyl substituted with at least one hydroxy. In an exemplary
embodiment, the compound is Formula (I), W, Y and Z are as
described herein, and said X is methyl substituted with at least
one hydroxy. In an exemplary embodiment, the compound is Formula
(I), W, Y and Z are as described herein, and said X is
hydroxymethyl.
[0085] In an exemplary embodiment, the compound is Formula (I), W,
Y and Z are as described herein, and said X is
##STR00043##
wherein R.sup.d is SH. In an exemplary embodiment, the compound is
Formula (I), W, Y and Z are as described herein, and said X is
##STR00044##
wherein R.sup.d is --SR.sup.15, wherein R.sup.15 is substituted or
unsubstituted alkyl. In an exemplary embodiment, the compound is
Formula (I), W, Y and Z are as described herein, and said X is
##STR00045##
wherein R.sup.d is --SR.sup.15, wherein R.sup.15 is unsubstituted
C.sub.1-C.sub.6 alkyl. In an exemplary embodiment, the compound is
Formula (I), W, Y and Z are as described herein, and said X is
##STR00046##
wherein R.sup.d is --SR.sup.15, wherein R.sup.15 is methyl. In an
exemplary embodiment, the compound is Formula (I), W, Y and Z are
as described herein, and said X is
##STR00047##
wherein R.sup.d is --SR.sup.15, wherein R.sup.15 is ethyl or propyl
or isopropyl.
[0086] In an exemplary embodiment, the compound is Formula (I), W,
Y and Z are as described herein, and said X is
##STR00048##
wherein R.sup.d is substituted or unsubstituted alkyl. In an
exemplary embodiment, the compound is Formula (I), W, Y and Z are
as described herein, and said X is
##STR00049##
wherein R.sup.d is unsubstituted C.sub.4-C.sub.6 alkyl. In an
exemplary embodiment, the compound is Formula (I), W, Y and Z are
as described herein, and said X is
##STR00050##
wherein R.sup.d is unsubstituted C.sub.2-C.sub.3 alkyl. In an
exemplary embodiment, the compound is Formula (I), W, Y and Z are
as described herein, and said X is
##STR00051##
wherein R.sup.d is methyl. In an exemplary embodiment, the compound
is Formula (I), W, Y and Z are as described herein, and said X
is
##STR00052##
wherein R.sup.d is ethyl or propyl or isopropyl. In an exemplary
embodiment, the compound is Formula (I), W, Y and Z are as
described herein, and said X is
##STR00053##
wherein R.sup.d is butyl, isobutyl, or t-butyl. In an exemplary
embodiment, the compound is Formula (I), W, Y and Z are as
described herein, and said X is
##STR00054##
wherein R.sup.d is C.sub.1-C.sub.6 alkyl, substituted with hydroxy.
In an exemplary embodiment, the compound is Formula (I), W, Y and Z
are as described herein, and said X is
##STR00055##
wherein R.sup.d is C.sub.1-C.sub.6 alkyl, substituted with
hydroxy.
[0087] In an exemplary embodiment, the compound is Formula (I), W,
Y and Z are as described herein, and said X is
##STR00056##
wherein R.sup.d is C.sub.1-C.sub.6 alkyl, substituted with
--OR.sup.20 or --SR.sup.20, wherein R.sup.20 is unsubstituted
C.sub.1-C.sub.6 alkyl. In an exemplary embodiment, the compound is
Formula (I), W, Y and Z are as described herein, and said X is
##STR00057##
wherein R.sup.d is C.sub.1-C.sub.2 alkyl, substituted with
--OR.sup.20 or --SR.sup.20, wherein R.sup.20 is unsubstituted
C.sub.1-C.sub.6 alkyl. In an exemplary embodiment, the compound is
Formula (I), W, Y and Z are as described herein, and said X is
##STR00058##
wherein R.sup.d is methyl, substituted with --OR.sup.20 or
--SR.sup.20, wherein R.sup.20 is unsubstituted C.sub.1-C.sub.6
alkyl. In an exemplary embodiment, the compound is Formula (I), W,
Y and Z are as described herein, and said X is
##STR00059##
wherein R.sup.d is C.sub.1-C.sub.6 alkyl, substituted with
--OR.sup.20 or --SR.sup.20, wherein R.sup.20 is unsubstituted
C.sub.1-C.sub.3 alkyl. In an exemplary embodiment, the compound is
Formula (I), W, Y and Z are as described herein, and said X is
##STR00060##
wherein R.sup.d is C.sub.1-C.sub.6 alkyl, substituted with
--OR.sup.20 or --SR.sup.20, wherein R.sup.20 is unsubstituted
C.sub.1-C.sub.2 alkyl. In an exemplary embodiment, the compound is
Formula (I), W, Y and Z are as described herein, and said X is
##STR00061##
wherein R.sup.d is C.sub.1-C.sub.6 alkyl, substituted with
--OR.sup.20 or --SR.sup.20, wherein R.sup.20 is methyl. In an
exemplary embodiment, the compound is Formula (I), W, Y and Z are
as described herein, and said X is
##STR00062##
wherein R.sup.d is methyl, substituted with --OR.sup.20 or
--SR.sup.20, wherein R.sup.20 is methyl.
[0088] In an exemplary embodiment, the compound is Formula (I), W,
Y and Z are as described herein, and said X is
##STR00063##
wherein R.sup.d is substituted alkenyl. In an exemplary embodiment,
the compound is Formula (I), W, Y and Z are as described herein,
and said X is unsubstituted alkenyl. In an exemplary embodiment,
the compound is Formula (I), W, Y and Z are as described herein,
and said R.sup.d is ethene. In an exemplary embodiment, the
compound is Formula (I), W, Y and Z are as described herein, and
said X is allyl.
[0089] In an exemplary embodiment, the compound is Formula (I), W,
Y and Z are as described herein, and said X is
##STR00064##
wherein R.sup.d is substituted alkynyl. In an exemplary embodiment,
the compound is Formula (I), W, Y and Z are as described herein,
and said X is
##STR00065##
wherein R.sup.d is ethynyl. In an exemplary embodiment, the
compound is Formula (I), W, Y and Z are as described herein, and
said X is unsubstituted alkynyl. In an exemplary embodiment, the
compound is Formula (I), W, Y and Z are as described herein, and
said X is propynyl. In an exemplary embodiment, the compound is
Formula (I), W, Y and Z are as described herein, and said X is
ethynyl.
[0090] In an exemplary embodiment, the compound is Formula (I), W,
Y and Z are as described herein, and said X is
##STR00066##
wherein R.sup.d is halogen. In an exemplary embodiment, the
compound is Formula (I), W, Y and Z are as described herein, and
said X is
##STR00067##
wherein R.sup.d is fluoro. In an exemplary embodiment, the compound
is Formula (I), W, Y and Z are as described herein, and said X
is
##STR00068##
wherein R.sup.d is chloro. In an exemplary embodiment, the compound
is Formula (I), W, Y and Z are as described herein, and said X
is
##STR00069##
wherein R.sup.d is bromo.
[0091] In an exemplary embodiment, the compound is Formula (I), W,
Y and Z are as described herein, and said X is
##STR00070##
wherein R.sup.d is substituted phenyl. In an exemplary embodiment,
the compound is Formula (I), W, Y and Z are as described herein,
and said X is
##STR00071##
wherein R.sup.d is unsubstituted phenyl.
[0092] In an exemplary embodiment, the compound is Formula (I), W,
Y and Z are as described herein, and said X is
##STR00072##
wherein R.sup.d and R.sup.e, along with the atom to which they are
connected, are optionally joined to form a substituted or
unsubstituted 3- to 8-membered ring. In an exemplary embodiment,
the compound is Formula (I), W, Y and Z are as described herein,
and said X is
##STR00073##
wherein R.sup.d and R.sup.e, along with the atom to which they are
connected, are optionally joined to form a substituted or
unsubstituted 3- to 6-membered ring. In an exemplary embodiment,
the compound is Formula (I), W, Y and Z are as described herein,
and said X is
##STR00074##
wherein R.sup.d and R.sup.e, along with the atom to which they are
connected, are optionally joined to form a unsubstituted 3- to
6-membered ring. In an exemplary embodiment, the compound is
Formula (I), W, Y and Z are as described herein, and said X is
##STR00075##
[0093] In an exemplary embodiment, the compound is Formula (I), W,
Y and Z are as described herein, and said X is
##STR00076##
wherein R.sup.c is --OR.sup.15, --NR.sup.15R.sup.16, --SR.sup.15,
--S(O)R.sup.15, --S(O).sub.2R.sup.15,
--S(O).sub.2NR.sup.15R.sup.16, --C(O)R.sup.15, --C(O)OR.sup.15, and
--C(O)NR.sup.15R.sup.16, wherein R.sup.15 and R.sup.16 are each
independently selected from the group consisting of H, halogen,
cyano, nitro, substituted or unsubstituted alkyl, substituted or
unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl,
substituted or unsubstituted heterocycloalkyl, substituted or
unsubstituted aryl, and substituted or unsubstituted heteroaryl,
and wherein R.sup.15 and R.sup.16, along with the nitrogen to which
they are connected, are optionally joined to form a substituted or
unsubstituted 4- to 8-membered ring. In an exemplary embodiment,
the compound is Formula (I), W, Y and Z are as described herein,
and said X is
##STR00077##
wherein R.sup.c is --OR.sup.15, wherein R.sup.15 is selected from
the group consisting of H, halogen, cyano, nitro, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl. In an exemplary
embodiment, the compound is Formula (I), W, Y and Z are as
described herein, and said X is
##STR00078##
wherein R.sup.c is --OR.sup.15, wherein R.sup.15 is selected from
the group consisting of H, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, and
substituted or unsubstituted heteroaryl. In an exemplary
embodiment, the compound is Formula (I), W, Y and Z are as
described herein, and said X is
##STR00079##
wherein R.sup.c is --OR.sup.15, wherein R.sup.15 is H. In an
exemplary embodiment, the compound is Formula (I), W, Y and Z are
as described herein, and said X is
##STR00080##
wherein R.sup.c is --OR.sup.15, wherein R.sup.15 is substituted
C.sub.1-C.sub.6 alkyl. In an exemplary embodiment, the compound is
Formula (I), W, Y and Z are as described herein, and said X is
##STR00081##
wherein R.sup.c is --OR.sup.15, wherein R.sup.15 is unsubstituted
C.sub.1-C.sub.6 alkyl. In an exemplary embodiment, the compound is
Formula (I), W, Y and Z are as described herein, and said X is
##STR00082##
wherein R.sup.c is --OR.sup.15, wherein R.sup.15 is unsubstituted
C.sub.1-C.sub.3 alkyl. In an exemplary embodiment the compound is
Formula (I), W, Y and Z are as described herein, and said X is
##STR00083##
wherein R.sup.c is --OR.sup.15, wherein R.sup.15 is methyl.
[0094] In an exemplary embodiment, the compound is Formula (I),
R.sup.4, R.sup.5, R.sup.6, R.sup.7, W, X and Y are as described
herein, Z is Formula (II) or (III), and R.sup.3 is H and R.sup.3a
is H. In an exemplary embodiment, the compound is Formula (I),
R.sup.4, R.sup.5, R.sup.6, R.sup.7, W, X and Y are as described
herein, Z is Formula (II) or (III), and R.sup.3 is unsubstituted
C.sub.1-C.sub.3 alkyl and R.sup.3a is unsubstituted C.sub.1-C.sub.3
alkyl. In an exemplary embodiment, the compound is Formula (I),
R.sup.4, R.sup.5, R.sup.6, R.sup.7, W, X and Y are as described
herein, Z is Formula (II) or (III), and R.sup.3 is unsubstituted
C.sub.1-C.sub.3 alkyl and R.sup.3a is H. In an exemplary
embodiment, the compound is Formula (I), R.sup.4, R.sup.5, R.sup.6,
R.sup.7, W, X and Y are as described herein, Z is Formula (II) or
(III), and R.sup.3 is methyl and R.sup.3a is methyl. In an
exemplary embodiment, the compound is Formula (I), R.sup.4,
R.sup.5, R.sup.6, R.sup.7, W, X and Y are as described herein, Z is
Formula (II) or (III), and R.sup.3 is methyl and R.sup.3a is H. In
an exemplary embodiment, the compound is Formula (I), R.sup.4,
R.sup.5, R.sup.6, R.sup.7, W, X and Y are as described herein, Z is
Formula (II) or (III), and R.sup.3 is C.sub.1-C.sub.3 alkyl
substituted with substituted or unsubstituted amino and R.sup.3a is
H. In an exemplary embodiment, the compound is Formula (I),
R.sup.4, R.sup.5, R.sup.6, R.sup.7, W, X and Y are as described
herein, Z is Formula (II) or (III), and R.sup.3 is
--CH.sub.2NH.sub.2 and R.sup.3a is H.
[0095] In an exemplary embodiment, the compound is Formula (I),
R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is Formula
(II), R.sup.4 is H or halogen, R.sup.5 is H or halogen, and R.sup.7
is H or halogen. In an exemplary embodiment, the compound is
Formula (I), R.sup.3, R.sup.3a, W, X and Y are as described herein,
Z is Formula (II), R.sup.4 is halogen, R.sup.5 is H, and R.sup.7 is
H. In an exemplary embodiment, the compound is Formula (I),
R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is Formula
(II), R.sup.4 is Cl, R.sup.5 is H, and R.sup.7 is H. In an
exemplary embodiment, the compound is Formula (I), R.sup.3,
R.sup.3a, W, X and Y are as described herein, Z is Formula (II),
R.sup.4 is F, R.sup.5 is H, and R.sup.7 is H. In an exemplary
embodiment, the compound is Formula (I), R.sup.3, R.sup.3a, W, X
and Y are as described herein, the compound is Formula (I), Z is
Formula (II), R.sup.4 is H, R.sup.5 is halogen, and R.sup.7 is H.
In an exemplary embodiment, the compound is Formula (I), R.sup.3,
R.sup.3a, W, X and Y are as described herein, Z is Formula (II),
R.sup.4 is H, R.sup.5 is Cl, and R.sup.7 is H. In an exemplary
embodiment, the compound is Formula (I), R.sup.3, R.sup.3a, W, X
and Y are as described herein, Z is Formula (II), R.sup.4 is H,
R.sup.5 is F, and R.sup.7 is H. In an exemplary embodiment, the
compound is Formula (I), R.sup.3, R.sup.3a, W, X and Y are as
described herein, Z is Formula (II), R.sup.4 is H, R.sup.5 is H,
and R.sup.7 is halogen. In an exemplary embodiment, the compound is
Formula (I), R.sup.3, R.sup.3a, W, X and Y are as described herein,
the compound is Formula (I), Z is Formula (II), R.sup.4 is H,
R.sup.5 is H, and R.sup.7 is Cl. In an exemplary embodiment, the
compound is Formula (I), R.sup.3, R.sup.3a, W, X and Y are as
described herein, Z is Formula (II), R.sup.4 is H, R.sup.5 is H,
and R.sup.7 is F. In an exemplary embodiment, the compound is
Formula (I), R.sup.3, R.sup.3a, W, X and Y are as described herein,
Z is Formula (II), R.sup.4 is H, R.sup.5 is halogen, and R.sup.7 is
halogen. In an exemplary embodiment, the compound is Formula (I),
R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is Formula
(II), R.sup.4 is H, R.sup.5 is Cl, and R.sup.7 is Cl. In an
exemplary embodiment, the compound is Formula (I), R.sup.3,
R.sup.3a, W, X and Y are as described herein, Z is Formula (II),
R.sup.4 is H, R.sup.5 is F, and R.sup.7 is F.
[0096] In an exemplary embodiment, the compound is Formula (I),
R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is Formula
(III), R.sup.4 is H or halogen, R.sup.6 is H or halogen, and
R.sup.7 is H or halogen. In an exemplary embodiment, the compound
is Formula (I), R.sup.3, R.sup.3a, W, X and Y are as described
herein, Z is Formula (III), R.sup.4 is halogen, R.sup.6 is H, and
R.sup.7 is H. In an exemplary embodiment, the compound is Formula
(I), R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is
Formula (III), R.sup.4 is Cl, R.sup.6 is H, and R.sup.7 is H. In an
exemplary embodiment, the compound is Formula (I), R.sup.3,
R.sup.3a, W, X and Y are as described herein, Z is Formula (III),
R.sup.4 is F, R.sup.6 is H, and R.sup.7 is H. In an exemplary
embodiment, the compound is Formula (I), R.sup.3, R.sup.3a, W, X
and Y are as described herein, Z is Formula (III), R.sup.4 is H,
R.sup.6 is halogen, and R.sup.7 is H. In an exemplary embodiment,
the compound is Formula (I), R.sup.3, R.sup.3a, W, X and Y are as
described herein, Z is Formula (III), R.sup.4 is H, R.sup.6 is Cl,
and R.sup.7 is H. In an exemplary embodiment, the compound is
Formula (I), R.sup.3, R.sup.3a, W, X and Y are as described herein,
Z is Formula (III), R.sup.4 is H, R.sup.6 is F, and R.sup.7 is H.
In an exemplary embodiment, the compound is Formula (I), R.sup.3,
R.sup.3a, W, X and Y are as described herein, Z is Formula (III),
R.sup.4 is H, R.sup.6 is H, and R.sup.7 is halogen. In an exemplary
embodiment, the compound is Formula (I), R.sup.3, R.sup.3a, W, X
and Y are as described herein, Z is Formula (III), R.sup.4 is H,
R.sup.6 is H, and R.sup.7 is Cl. In an exemplary embodiment, the
compound is Formula (I), R.sup.3, R.sup.3a, W, X and Y are as
described herein, Z is Formula (III), R.sup.4 is H, R.sup.6 is H,
and R.sup.7 is F. In an exemplary embodiment, the compound is
Formula (I), R.sup.3, R.sup.3a, W, X and Y are as described herein,
Z is Formula (III), R.sup.4 is H, R.sup.6 is halogen, and R.sup.7
is halogen. In an exemplary embodiment, the compound is Formula
(I), R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is
Formula (III), R.sup.4 is H, R.sup.6 is Cl, and R.sup.7 is Cl. In
an exemplary embodiment, the compound is Formula (I), R.sup.3,
R.sup.3a, W, X and Y are as described herein, Z is Formula (III),
R.sup.4 is H, R.sup.6 is F, and R.sup.7 is F.
[0097] In an exemplary embodiment, the compound is Formula (I),
R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is Formula
(II), R.sup.4 is H or cyano, R.sup.5 is H or cyano, and R.sup.7 is
H or cyano. In an exemplary embodiment, the compound is Formula
(I), R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is
Formula (II), R.sup.4 is cyano, R.sup.5 is H, and R.sup.7 is H. In
an exemplary embodiment, the compound is Formula (I), R.sup.3,
R.sup.3a, W, X and Y are as described herein, Z is Formula (II),
R.sup.4 is H, R.sup.5 is cyano, and R.sup.7 is H. In an exemplary
embodiment, the compound is Formula (I), R.sup.3, R.sup.3a, W, X
and Y are as described herein, Z is Formula (II), R.sup.4 is H,
R.sup.5 is H, and R.sup.7 is cyano.
[0098] In an exemplary embodiment, the compound is Formula (I),
R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is Formula
(III), R.sup.4 is H or cyano, R.sup.6 is H or cyano, and R.sup.7 is
H or cyano. In an exemplary embodiment, the compound is Formula
(I), R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is
Formula (III), R.sup.4 is cyano, R.sup.6 is H, and R.sup.7 is H. In
an exemplary embodiment, the compound is Formula (I), R.sup.3,
R.sup.3a, W, X and Y are as described herein, Z is Formula (III),
R.sup.4 is H, R.sup.6 is cyano, and R.sup.7 is H. In an exemplary
embodiment, the compound is Formula (I), R.sup.3, R.sup.3a, W, X
and Y are as described herein, Z is Formula (III), R.sup.4 is H,
R.sup.6 is H, and R.sup.7 is cyano.
[0099] In an exemplary embodiment, the compound is Formula (I),
R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is Formula
(II), R.sup.4, R.sup.5, and R.sup.7 are each independently selected
from H or C.sub.1-C.sub.3 alkyl substituted with amino. In an
exemplary embodiment, the compound is Formula (I), R.sup.3,
R.sup.3a, W, X and Y are as described herein, Z is Formula (II),
R.sup.4, R.sup.5, and R.sup.7 are each independently selected from
H or --CH.sub.2NH.sub.2. In an exemplary embodiment, the compound
is Formula (I), R.sup.3, R.sup.3a, W, X and Y are as described
herein, Z is Formula (II), R.sup.4 is --CH.sub.2NH.sub.2, R.sup.5
is H, and R.sup.7 is H. In an exemplary embodiment, the compound is
Formula (I), R.sup.3, R.sup.3a, W, X and Y are as described herein,
Z is Formula (II), R.sup.4 is H, R.sup.5 is --CH.sub.2NH.sub.2, and
R.sup.7 is H. In an exemplary embodiment, the compound is Formula
(I), R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is
Formula (II), R.sup.4 is H, R.sup.5 is H, and R.sup.7 is
--CH.sub.2NH.sub.2.
[0100] In an exemplary embodiment, the compound is Formula (I),
R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is Formula
(III), R.sup.4, R.sup.6, and R.sup.7 are each independently
selected from H or C.sub.1-C.sub.3 alkyl substituted with amino. In
an exemplary embodiment, the compound is Formula (I), R.sup.3,
R.sup.3a, W, X and Y are as described herein, Z is Formula (III),
R.sup.4, R.sup.6, and R.sup.7 are each independently selected from
H or --CH.sub.2NH.sub.2. In an exemplary embodiment, the compound
is Formula (I), R.sup.3, R.sup.3a, W, X and Y are as described
herein, Z is Formula (III), R.sup.4 is --CH.sub.2NH.sub.2, R.sup.6
is H, and R.sup.7 is H. In an exemplary embodiment, the compound is
Formula (I), R.sup.3, R.sup.3a, W, X and Y are as described herein,
Z is Formula (III), R.sup.4 is H, R.sup.6 is --CH.sub.2NH.sub.2,
and R.sup.7 is H. In an exemplary embodiment, the compound is
Formula (I), R.sup.3, R.sup.3a, W, X and Y are as described herein,
Z is Formula (III), R.sup.4 is H, R.sup.6 is H, and R.sup.7 is
--CH.sub.2NH.sub.2.
[0101] In an exemplary embodiment, the compound is Formula (I),
R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is Formula
(II), R.sup.4, R.sup.5, and R.sup.7 are each independently selected
from H or C.sub.1-C.sub.3 alkoxy. In an exemplary embodiment, the
compound is Formula (I), R.sup.3, R.sup.3a, W, X and Y are as
described herein, Z is Formula (II), R.sup.4, R.sup.5, and R.sup.7
are each independently selected from H or --OCH.sub.3. In an
exemplary embodiment, the compound is Formula (I), R.sup.3,
R.sup.3a, W, X and Y are as described herein, Z is Formula (II),
R.sup.4 is --OCH.sub.3, R.sup.5 is H, and R.sup.7 is H. In an
exemplary embodiment, the compound is Formula (I), R.sup.3,
R.sup.3a, W, X and Y are as described herein, Z is Formula (II),
R.sup.4 is H, R.sup.5 is --OCH.sub.3, and R.sup.7 is H. In an
exemplary embodiment, the compound is Formula (I), R.sup.3,
R.sup.3a, W, X and Y are as described herein, Z is Formula (II),
R.sup.4 is H, R.sup.5 is H, and R.sup.7 is --OCH.sub.3.
[0102] In an exemplary embodiment, the compound is Formula (I),
R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is Formula
(III), R.sup.4, R.sup.6, and R.sup.7 are each independently
selected from H or C.sub.1-C.sub.3 alkoxy. In an exemplary
embodiment, the compound is Formula (I), R.sup.3, R.sup.3a, W, X
and Y are as described herein, Z is Formula (III), R.sup.4,
R.sup.6, and R.sup.7 are each independently selected from H or
--OCH.sub.3. In an exemplary embodiment, the compound is Formula
(I), R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is
Formula (III), R.sup.4 is --OCH.sub.3, R.sup.6 is H, and R.sup.7 is
H. In an exemplary embodiment, the compound is Formula (I),
R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is Formula
(III), R.sup.4 is H, R.sup.6 is --OCH.sub.3, and R.sup.7 is H. In
an exemplary embodiment, the compound is Formula (I), R.sup.3,
R.sup.3a, W, X and Y are as described herein, Z is Formula (III),
R.sup.4 is H, R.sup.6 is H, and R.sup.7 is --OCH.sub.3.
[0103] In an exemplary embodiment, the compound is Formula (I),
R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is Formula
(II), R.sup.4 is H, R.sup.5 is H, and R.sup.7 is H. In an exemplary
embodiment, the compound is Formula (I), W, X and Y are as
described herein, Z is Formula (II), R.sup.3 is H, R.sup.3a is H,
R.sup.4 is H, R.sup.5 is H, and R.sup.7 is H. In an exemplary
embodiment, the compound is Formula (I), W, X and Y are as
described herein, Z is Formula (II), R.sup.3 is CH.sub.3, R.sup.3a
is H, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is H. In an exemplary
embodiment, the compound is Formula (I), W, X and Y are as
described herein, Z is Formula (II), R.sup.3 is CH.sub.3, R.sup.3a
is CH.sub.3, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is H. In an
exemplary embodiment the compound is Formula (I), W, X and Y are as
described herein, Z is Formula (II), R.sup.3 is --CH.sub.2NH.sub.2,
R.sup.3a is H, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is H.
[0104] In an exemplary embodiment, the compound is Formula (I),
R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is Formula
(III), R.sup.4 is H, R.sup.6 is H, and R.sup.7 is H. In an
exemplary embodiment, the compound is Formula (I), W, X and Y are
as described herein, Z is Formula (III), R.sup.3 is H, R.sup.3a is
H, R.sup.4 is H, R.sup.6 is H, and R.sup.7 is H. In an exemplary
embodiment, the compound is Formula (I), W, X and Y are as
described herein, Z is Formula (III), R.sup.3 is CH.sub.3, R.sup.3a
is H, R.sup.4 is H, R.sup.6 is H, and R.sup.7 is H. In an exemplary
embodiment, the compound is Formula (I), W, X and Y are as
described herein, Z is Formula (III), R.sup.3 is CH.sub.3, R.sup.3a
is CH.sub.3, R.sup.4 is H, R.sup.6 is H, and R.sup.7 is H. In an
exemplary embodiment, the compound is Formula (I), W, X and Y are
as described herein, Z is Formula (III), R.sup.3 is
--CH.sub.2NH.sub.2, R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and
R.sup.7 is H.
[0105] In an exemplary embodiment, the compound is Formula (I),
R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is Formula
(II), R.sup.4 is H, R.sup.5 is H, and R.sup.7 is F. In an exemplary
embodiment, the compound is Formula (I), W, X and Y are as
described herein, Z is Formula (II), R.sup.3 is H, R.sup.3a is H,
R.sup.4 is H, R.sup.5 is H, and R.sup.7 is F. In an exemplary
embodiment, the compound is Formula (I), W, X and Y are as
described herein, Z is Formula (II), R.sup.3 is CH.sub.3, R.sup.3a
is H, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is F. In an exemplary
embodiment, the compound is Formula (I), W, X and Y are as
described herein, Z is Formula (II), R.sup.3 is CH.sub.3, R.sup.3a
is CH.sub.3, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is F. In an
exemplary embodiment, the compound is Formula (I), W, X and Y are
as described herein, Z is Formula (II), R.sup.3 is
--CH.sub.2NH.sub.2, R.sup.3a is H, R.sup.4 is H, R.sup.5 is H, and
R.sup.7 is F.
[0106] In an exemplary embodiment, the compound is Formula (I),
R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is Formula
(III), R.sup.4 is H, R.sup.6 is H, and R.sup.7 is F. In an
exemplary embodiment, the compound is Formula (I), W, X and Y are
as described herein, Z is Formula (III), R.sup.3 is H, R.sup.3a is
H, R.sup.4 is H, R.sup.6 is H, and R.sup.7 is F. In an exemplary
embodiment, the compound is Formula (I), W, X and Y are as
described herein, Z is Formula (III), R.sup.3 is CH.sub.3, R.sup.3a
is H, R.sup.4 is H, R.sup.6 is H, and R.sup.7 is F. In an exemplary
embodiment, the compound is Formula (I), W, X and Y are as
described herein, Z is Formula (III), R.sup.3 is CH.sub.3, R.sup.3a
is CH.sub.3, R.sup.4 is H, R.sup.6 is H, and R.sup.7 is F. In an
exemplary embodiment, the compound is Formula (I), W, X and Y are
as described herein, Z is Formula (III), R.sup.3 is
--CH.sub.2NH.sub.2, R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and
R.sup.7 is F.
[0107] In an exemplary embodiment, the compound is Formula (I),
R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is Formula
(II), R.sup.4 is H, R.sup.5 is F, and R.sup.7 is H. In an exemplary
embodiment, the compound is Formula (I), W, X and Y are as
described herein, Z is Formula (II), R.sup.3 is H, R.sup.3a is H,
R.sup.4 is H, R.sup.5 is F, and R.sup.7 is H. In an exemplary
embodiment, the compound is Formula (I), W, X and Y are as
described herein, Z is Formula (II), R.sup.3 is CH.sub.3, R.sup.3a
is H, R.sup.4 is H, R.sup.5 is F, and R.sup.7 is H. In an exemplary
embodiment, the compound is Formula (I), W, X and Y are as
described herein, Z is Formula (II), R.sup.3 is CH.sub.3, R.sup.3a
is CH.sub.3, R.sup.4 is H, R.sup.5 is F, and R.sup.7 is H. In an
exemplary embodiment, the compound is Formula (I), W, X and Y are
as described herein, Z is Formula (II), R.sup.3 is
--CH.sub.2NH.sub.2, R.sup.3a is H, R.sup.4 is H, R.sup.5 is F, and
R.sup.7 is H.
[0108] In an exemplary embodiment, the compound is Formula (I),
R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is Formula
(III), R.sup.4 is H, R.sup.6 is F, and R.sup.7 is H. In an
exemplary embodiment, the compound is Formula (I), W, X and Y are
as described herein, Z is Formula (III), R.sup.3 is H, R.sup.3a is
H, R.sup.4 is H, R.sup.6 is F, and R.sup.7 is H. In an exemplary
embodiment, the compound is Formula (I), W, X and Y are as
described herein, Z is Formula (III), R.sup.3 is CH.sub.3, R.sup.3a
is H, R.sup.4 is H, R.sup.6 is F, and R.sup.7 is H. In an exemplary
embodiment, the compound is Formula (I), W, X and Y are as
described herein, Z is Formula (III), R.sup.3 is CH.sub.3, R.sup.3a
is CH.sub.3, R.sup.4 is H, R.sup.6 is F, and R.sup.7 is H. In an
exemplary embodiment, the compound is Formula (I), W, X and Y are
as described herein, Z is Formula (III), R.sup.3 is
--CH.sub.2NH.sub.2, R.sup.3a is H, R.sup.4 is H, R.sup.6 is F, and
R.sup.7 is H.
[0109] In an exemplary embodiment, the compound is Formula (I),
R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is Formula
(II), R.sup.4 is H, R.sup.5 is H, and R.sup.7 is CN. In an
exemplary embodiment, the compound is Formula (I), W, X and Y are
as described herein, Z is Formula (II), R.sup.3 is H, R.sup.3a is
H, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is CN. In an exemplary
embodiment, the compound is Formula (I), W, X and Y are as
described herein, Z is Formula (II), R.sup.3 is CH.sub.3, R.sup.3a
is H, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is CN. In an
exemplary embodiment, the compound is Formula (I), W, X and Y are
as described herein, Z is Formula (II), R.sup.3 is CH.sub.3,
R.sup.3a is CH.sub.3, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is
CN. In an exemplary embodiment, the compound is Formula (I), W, X
and Y are as described herein, Z is Formula (II), R.sup.3 is
--CH.sub.2NH.sub.2, R.sup.3a is H, R.sup.4 is H, R.sup.5 is H, and
R.sup.7 is CN.
[0110] In an exemplary embodiment, the compound is Formula (I),
R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is Formula
(III), R.sup.4 is H, R.sup.6 is H, and R.sup.7 is CN. In an
exemplary embodiment, the compound is Formula (I), W, X and Y are
as described herein, Z is Formula (III), R.sup.3 is H, R.sup.3a is
H, R.sup.4 is H, R.sup.6 is H, and R.sup.7 is CN. In an exemplary
embodiment, the compound is Formula (I), W, X and Y are as
described herein, Z is Formula (III), R.sup.3 is CH.sub.3, R.sup.3a
is H, R.sup.4 is H, R.sup.6 is H, and R.sup.7 is CN. In an
exemplary embodiment, the compound is Formula (I), W, X and Y are
as described herein, Z is Formula (III), R.sup.3 is CH.sub.3,
R.sup.3a is CH.sub.3, R.sup.4 is H, R.sup.6 is H, and R.sup.7 is
CN. In an exemplary embodiment, the compound is Formula (I), W, X
and Y are as described herein, Z is Formula (III), R.sup.3 is
--CH.sub.2NH.sub.2, R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and
R.sup.7 is CN.
[0111] In an exemplary embodiment, the compound is Formula (I),
R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is Formula
(II), R.sup.4 is H, R.sup.5 is --OCH.sub.3, and R.sup.7 is H. In an
exemplary embodiment, the compound is Formula (I), W, X and Y are
as described herein, Z is Formula (II), R.sup.3 is H, R.sup.3a is
H, R.sup.4 is H, R.sup.5 is --OCH.sub.3, and R.sup.7 is H. In an
exemplary embodiment, the compound is Formula (I), W, X and Y are
as described herein, Z is Formula (II), R.sup.3 is CH.sub.3,
R.sup.3a is H, R.sup.4 is H, R.sup.5 is --OCH.sub.3, and R.sup.7 is
H. In an exemplary embodiment, the compound is Formula (I), W, X
and Y are as described herein, Z is Formula (II), R.sup.3 is
CH.sub.3, R.sup.3a is CH.sub.3, R.sup.4 is H, R.sup.5 is
--OCH.sub.3, and R.sup.7 is H. In an exemplary embodiment, the
compound is Formula (I), W, X and Y are as described herein, Z is
Formula (II), R.sup.3 is --CH.sub.2NH.sub.2, R.sup.3a is H, R.sup.4
is H, R.sup.5 is --OCH.sub.3, and R.sup.7 is H.
[0112] In an exemplary embodiment, the compound is Formula (I),
R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is Formula
(III), R.sup.4 is H, R.sup.6 is --OCH.sub.3, and R.sup.7 is H. In
an exemplary embodiment, the compound is Formula (I), W, X and Y
are as described herein, Z is Formula (III), R.sup.3 is H, R.sup.3a
is H, R.sup.4 is H, R.sup.6 is --OCH.sub.3, and R.sup.7 is H. In an
exemplary embodiment, the compound is Formula (I), W, X and Y are
as described herein, Z is Formula (III), R.sup.3 is CH.sub.3,
R.sup.3a is H, R.sup.4 is H, R.sup.6 is --OCH.sub.3, and R.sup.7 is
H. In an exemplary embodiment, the compound is Formula (I), W, X
and Y are as described herein, Z is Formula (III), R.sup.3 is
CH.sub.3, R.sup.3a is CH.sub.3, R.sup.4 is H, R.sup.6 is
--OCH.sub.3, and R.sup.7 is H. In an exemplary embodiment, the
compound is Formula (I), W, X and Y are as described herein, Z is
Formula (III), R.sup.3 is --CH.sub.2NH.sub.2, R.sup.3a is H,
R.sup.4 is H, R.sup.6 is --OCH.sub.3, and R.sup.7 is H.
[0113] In an exemplary embodiment, the compound is Formula (I),
R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is Formula
(II), R.sup.4 is --CH.sub.2NH.sub.2, R.sup.5 is H, and R.sup.7 is
H. In an exemplary embodiment, the compound is Formula (I), W, X
and Y are as described herein, Z is Formula (II), R.sup.3 is H,
R.sup.3a is H, R.sup.4 is --CH.sub.2NH.sub.2, R.sup.5 is H, and
R.sup.7 is H. In an exemplary embodiment, the compound is Formula
(I), W, X and Y are as described herein, Z is Formula (II), R.sup.3
is CH.sub.3, R.sup.3a is H, R.sup.4 is --CH.sub.2NH.sub.2, R.sup.5
is H, and R.sup.7 is H. In an exemplary embodiment, the compound is
Formula (I), W, X and Y are as described herein, Z is Formula (II),
R.sup.3 is CH.sub.3, R.sup.3a is CH.sub.3, R.sup.4 is
--CH.sub.2NH.sub.2, R.sup.5 is H, and R.sup.7 is H. In an exemplary
embodiment, the compound is Formula (I), W, X and Y are as
described herein, Z is Formula (II), R.sup.3 is --CH.sub.2NH.sub.2,
R.sup.3a is H, R.sup.4 is --CH.sub.2NH.sub.2, R.sup.5 is H, and
R.sup.7 is H.
[0114] In an exemplary embodiment, the compound is Formula (I),
R.sup.3, R.sup.3a, W, X and Y are as described herein, Z is Formula
(III), R.sup.4 is --CH.sub.2NH.sub.2, R.sup.6 is H, and R.sup.7 is
H. In an exemplary embodiment, the compound is Formula (I), W, X
and Y are as described herein, Z is Formula (III), R.sup.3 is H,
R.sup.3a is H, R.sup.4 is --CH.sub.2NH.sub.2, R.sup.6 is H, and
R.sup.7 is H. In an exemplary embodiment, the compound is Formula
(I), W, X and Y are as described herein, Z is Formula (III),
R.sup.3 is CH.sub.3, R.sup.3a is H, R.sup.4 is --CH.sub.2NH.sub.2,
R.sup.6 is H, and R.sup.7 is H. In an exemplary embodiment, the
compound is Formula (I), W, X and Y are as described herein, Z is
Formula (III), R.sup.3 is CH.sub.3, R.sup.3a is CH.sub.3, R.sup.4
is --CH.sub.2NH.sub.2, R.sup.6 is H, and R.sup.7 is H. In an
exemplary embodiment, the compound is Formula (I), W, X and Y are
as described herein, Z is Formula (III), R.sup.3 is
--CH.sub.2NH.sub.2, R.sup.3a is H, R.sup.4 is --CH.sub.2NH.sub.2,
R.sup.6 is H, and R.sup.7 is H.
[0115] In an exemplary embodiment, the compound is Formula (I), W,
X and Y are as described herein, and said Z is
##STR00084##
wherein R.sup.3, R.sup.3a, R.sup.4, and R.sup.7 are each
independently selected from the group consisting of R.sup.10,
--OR.sup.10, --NR.sup.10R.sup.11, --SR.sup.10, --S(O)R.sup.10,
--S(O).sub.2R.sup.10, --S(O).sub.2NR.sup.10R.sup.11,
--C(O)R.sup.10, --C(O)OR.sup.10, and --C(O)NR.sup.10R.sup.11
wherein R.sup.10 and R.sup.11 are each independently selected from
the group consisting of H, halogen, cyano, nitro, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl.
[0116] In an exemplary embodiment, the compound is Formula (I), W,
X and Y are as described herein, and said Z is
##STR00085##
wherein R.sup.3, R.sup.3a, R.sup.5, and R.sup.7 are each
independently selected from the group consisting of R.sup.10,
--OR.sup.10, --NR.sup.10R.sup.11, --SR.sup.10, --S(O)R.sup.10,
--S(O).sub.2R.sup.10, --S(O).sub.2NR.sup.10R.sup.11,
--C(O)R.sup.10, --C(O)OR.sup.10, and --C(O)NR.sup.10R.sup.11
wherein R.sup.10 and R.sup.11 are each independently selected from
the group consisting of H, halogen, cyano, nitro, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl.
[0117] In an exemplary embodiment, the compound is Formula (I), W,
X and Y are as described herein, and said Z is
##STR00086##
wherein R.sup.3, R.sup.3a, R.sup.4, R.sup.5, and R.sup.7 are each
independently selected from the group consisting of R.sup.10,
--OR.sup.10, --NR.sup.10OR.sup.11, --SR.sup.10, --S(O)R.sup.10,
--S(O).sub.2R'.degree., --S(O).sub.2NR.sup.10R.sup.11,
--C(O)R.sup.10, --C(O)OR.sup.10, and --C(O)NR.sup.10R.sup.11
wherein R.sup.10 and R.sup.11 are each independently selected from
the group consisting of H, halogen, cyano, nitro, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl.
[0118] In an exemplary embodiment, the compound is Formula (I), W,
X and Y are as described herein, and said Z is
##STR00087##
wherein R.sup.3, R.sup.3a, R.sup.4, R.sup.6, and R.sup.7 are each
independently selected from the group consisting of R.sup.10,
--OR.sup.10, --NR.sup.10R.sup.11, --SR.sup.10, --S(O)R.sup.10,
--S(O).sub.2R.sup.10, --S(O).sub.2NR.sup.10R.sup.11,
--C(O)R.sup.10, --C(O)OR.sup.10, and --C(O)NR.sup.10R.sup.11
wherein R.sup.10 and R.sup.11 are each independently selected from
the group consisting of H, halogen, cyano, nitro, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl.
[0119] In an exemplary embodiment, the compound is Formula (I), W,
X and Y are as described herein, and said Z is
##STR00088##
wherein R.sup.3, R.sup.3a, R.sup.4, R.sup.5, and R.sup.7 are each
independently selected from the group consisting of R.sup.10,
--OR.sup.10, --NR.sup.10R.sup.11, --SR.sup.10, --S(O)R.sup.10,
--S(O).sub.2R'.degree., --S(O).sub.2NR.sup.10R.sup.11,
--C(O)R.sup.10, --C(O)OR.sup.10, and --C(O)NR.sup.10R.sup.11
wherein R.sup.10 and R.sup.11 are each independently selected from
the group consisting of H, halogen, cyano, nitro, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl.
[0120] In an exemplary embodiment, the compound is Formula (I), W,
X and Y are as described herein, and said Z is
##STR00089##
wherein R.sup.3, R.sup.3a, R.sup.4, R.sup.6, and R.sup.7 are each
independently selected from the group consisting of R.sup.10,
--OR.sup.10, --NR.sup.10R.sup.11, --SR.sup.10, --S(O)R.sup.10,
--S(O).sub.2R.sup.10, --S(O).sub.2NR.sup.10R.sup.11,
--C(O)R.sup.10, --C(O)OR.sup.10, and --C(O)NR.sup.10R.sup.11
wherein R.sup.10 and R.sup.11 are each independently selected from
the group consisting of H, halogen, cyano, nitro, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl.
[0121] In an exemplary embodiment, the compound is Formula (I), W,
X and Y are as described herein, and said Z is
##STR00090##
wherein R.sup.1, R.sup.4, R.sup.5, and R.sup.7 are each
independently selected from the group consisting of R.sup.10,
--OR.sup.10, --NR.sup.10R.sup.11, --SR.sup.10, --S(O)R.sup.10,
--S(O).sub.2R.sup.10, --S(O).sub.2NR.sup.10R.sup.11,
--C(O)R.sup.10, --C(O)OR.sup.10, and --C(O)NR.sup.10R.sup.11
wherein R.sup.10 and R.sup.11 are each independently selected from
the group consisting of H, halogen, cyano, nitro, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl.
[0122] In an exemplary embodiment, the compound is Formula (I), W,
X and Y are as described herein, and said Z is
##STR00091##
wherein R.sup.1, R.sup.4, R.sup.6, and R.sup.7 are each
independently selected from the group consisting of R.sup.10,
--OR.sup.10, --NR.sup.10R.sup.11, --SR.sup.10, --S(O)R.sup.10,
--S(O).sub.2R.sup.10, --S(O).sub.2NR.sup.10R.sup.11,
--C(O)R.sup.10, --C(O)OR.sup.10, and --C(O)NR.sup.10R.sup.11
wherein R.sup.10 and R.sup.11 are each independently selected from
the group consisting of H, halogen, cyano, nitro, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl.
[0123] In an exemplary embodiment, the compound is Formula (I), W,
X and Y are as described herein, and said Z is
##STR00092##
wherein R.sup.3 and R.sup.3a are each independently selected from
the group consisting of R, --OR.sup.10, --NROR.sup.11, --SR.sup.10,
--S(O)R.sup.10, --S(O).sub.2R.sup.10,
--S(O).sub.2NR.sup.10R.sup.11, --C(O)R.sup.10, --C(O)OR.sup.10, and
--C(O)NR.sup.10R.sup.11 wherein R.sup.10 and R.sup.11 are each
independently selected from the group consisting of H, halogen,
cyano, nitro, substituted or unsubstituted alkyl, substituted or
unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl,
substituted or unsubstituted heterocycloalkyl, substituted or
unsubstituted aryl, and substituted or unsubstituted
heteroaryl.
[0124] In an exemplary embodiment, the compound is Formula (I), W,
X and Y are as described herein, and said Z is
##STR00093##
wherein R.sup.1, R.sup.4, R.sup.5, and R.sup.7 are each
independently selected from the group consisting of R.sup.10,
--OR.sup.10, --NROR.sup.11, --SR.sup.10, --S(O)R.sup.10,
--S(O).sub.2R.sup.10, --S(O).sub.2NR.sup.10R.sup.11,
--C(O)R.sup.10, --C(O)OR.sup.10, and --C(O)NR.sup.10R.sup.11
wherein R.sup.10 and R.sup.11 are each independently selected from
the group consisting of H, halogen, cyano, nitro, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl.
[0125] In an exemplary embodiment, the compound is Formula (I), W
is H, and X, Y, and Z are as described herein. In an exemplary
embodiment, the compound is Formula (I), X and Z are as described
herein, W is H, and Y is substituted alkylene. In an exemplary
embodiment, the compound is Formula (I), X and Z are as described
herein, W is H, and Y is unsubstituted alkylene. In an exemplary
embodiment, the compound is Formula (I), X and Z are as described
herein, W is H, and Y is methylene. In an exemplary embodiment, the
compound is Formula (I), X and Z are as described herein, W is H,
and Y is ethylene. In an exemplary embodiment, the compound is
Formula (I), X and Z are as described herein, W is H, and Y is
propylene. In an exemplary embodiment, the compound is Formula (I),
X and Z are as described herein, W is H, and Y is substituted
heteroalkylene. In an exemplary embodiment, the compound is Formula
(I), X and Z are as described herein, W is H, and Y is
unsubstituted heteroalkylene. In an exemplary embodiment, the
compound is Formula (I), X and Z are as described herein, W is H,
and Y is *--OCH.sub.2--. In an exemplary embodiment, the compound
is Formula (I), X and Z are as described herein, W is H, and Y is
*--SCH.sub.2--. In an exemplary embodiment, the compound is Formula
(I), X and Z are as described herein, W is H, and Y is
*--NHCH.sub.2--. In an exemplary embodiment, the compound is
Formula (I), X and Z are as described herein, W is H, and Y is
*--CH.sub.2NH--. In an exemplary embodiment, the compound is
Formula (I), X and Z are as described herein, W is H, and Y is
*--C(O)NH--. In an exemplary embodiment, the compound is Formula
(I), X and Z are as described herein, W is H, and Y is
*--CH.sub.2NHCH.sub.2-- or 1-piperazinyl or *--S(O)CH.sub.2-- or
*--S(O).sub.2--. In an exemplary embodiment, the compound is
Formula (I), X and Z are as described herein, W is H, and Y is
1-piperazinyl. In an exemplary embodiment, the compound is Formula
(I), X and Z are as described herein, W is H, and Y is
*--S(O)CH.sub.2--. In an exemplary embodiment, the compound is
Formula (I), X and Z are as described herein, W is H, and Y is
*--S(O).sub.2--. In an exemplary embodiment, the compound is
Formula (I), X and Z are as described herein, W is H, and Y is
*--S(O).sub.2CH.sub.2--. In an exemplary embodiment, the compound
is Formula (I), X and Z are as described herein, W is H, and Y is
*--NHC(O)OCH.sub.2--. In this paragraph, * represents the point of
attachment to Z.
[0126] In an exemplary embodiment, the compound is Formula (I), W
is H, X and Y are as described herein, and Z is substituted or
unsubstituted heteroaryl, wherein said heteroaryl comprises an
endocyclic boron. In an exemplary embodiment, the compound is
Formula (I), W is H, X and Y are as described herein, and Z is
substituted or unsubstituted heteroaryl, wherein said heteroaryl
has one ring, and said ring comprises an endocyclic boron. In an
exemplary embodiment, the compound is Formula (I), W is H, X and Y
are as described herein, and Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl has two rings, and one of the
two rings comprises an endocyclic boron.
[0127] In an exemplary embodiment, the compound is Formula (I), W
is H, X and Y are as described herein, and Z is substituted or
unsubstituted heterocycloalkyl, wherein said heterocycloalkyl
comprises an endocyclic boron. In an exemplary embodiment, the
compound is Formula (I), W is H, X and Y are as described herein,
and Z is substituted or unsubstituted heterocycloalkyl, wherein
said heterocycloalkyl has one ring, and said ring comprises an
endocyclic boron. In an exemplary embodiment, the compound is
Formula (I), W is H, X and Y are as described herein, and Z is
substituted or unsubstituted heterocycloalkyl, wherein said
heterocycloalkyl has two rings, and one of the two rings comprises
an endocyclic boron.
[0128] In an exemplary embodiment, the compound is Formula (I), W
is H, X and Y are as described herein, and Z is substituted or
unsubstituted benzoxaborole. In an exemplary embodiment, the
compound is Formula (I), W is H, X and Y are as described herein,
and Z is substituted or unsubstituted pyridinyloxaborole. In an
exemplary embodiment, the compound is Formula (I), W is H, X and Y
are as described herein, and Z is substituted or unsubstituted
benzoxaborininol. In an exemplary embodiment, the compound is
Formula (I), W is H, X and Y are as described herein, and Z is
substituted or unsubstituted benzoxazaborininol. In an exemplary
embodiment, the compound is Formula (I), W is H, X and Y are as
described herein, and Z is substituted or unsubstituted
benzodiazaborininol. In an exemplary embodiment, the compound is
Formula (I), W is H, X and Y are as described herein, and Z is
substituted or unsubstituted oxaborole. In an exemplary embodiment,
the compound is Formula (I), W is H, X and Y are as described
herein, and Z is substituted or unsubstituted
dihydrobenzoazaborinine.
[0129] In an exemplary embodiment, the compound is Formula (I), X
is as described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl comprises an endocyclic boron,
and Y is substituted alkylene. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heteroaryl, wherein said heteroaryl
comprises an endocyclic boron, and Y is unsubstituted alkylene. In
an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl comprises an endocyclic boron,
and Y is methylene. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is substituted or
unsubstituted heteroaryl, wherein said heteroaryl comprises an
endocyclic boron, and Y is ethylene. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heteroaryl, wherein said heteroaryl
comprises an endocyclic boron, and Y is propylene. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is substituted or unsubstituted heteroaryl, wherein said
heteroaryl comprises an endocyclic boron, and Y is substituted
heteroalkylene. In an exemplary embodiment, the compound is Formula
(I), X is as described herein, W is H, Z is substituted or
unsubstituted heteroaryl, wherein said heteroaryl comprises an
endocyclic boron, and Y is unsubstituted heteroalkylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl comprises an endocyclic boron,
and Y is *--OCH.sub.2--. In an exemplary embodiment, the compound
is Formula (I), X is as described herein, W is H, Z is substituted
or unsubstituted heteroaryl, wherein said heteroaryl comprises an
endocyclic boron, and Y is *--SCH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is substituted or unsubstituted heteroaryl, wherein said
heteroaryl comprises an endocyclic boron, and Y is *--NHCH.sub.2--.
In an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl comprises an endocyclic boron,
and Y is *--CH.sub.2NH--. In an exemplary embodiment, the compound
is Formula (I), X is as described herein, W is H, Z is substituted
or unsubstituted heteroaryl, wherein said heteroaryl comprises an
endocyclic boron, and Y is *--C(O)NH--. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heteroaryl, wherein said heteroaryl
comprises an endocyclic boron, and Y is *--CH.sub.2NHCH.sub.2-- or
1-piperazinyl or *--S(O)CH.sub.2-- or *--S(O).sub.2--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl comprises an endocyclic boron,
and Y is 1-piperazinyl. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is substituted or
unsubstituted heteroaryl, wherein said heteroaryl comprises an
endocyclic boron, and Y is *--S(O)CH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is substituted or unsubstituted heteroaryl, wherein said
heteroaryl comprises an endocyclic boron, and Y is *--S(O).sub.2--.
In an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl comprises an endocyclic boron,
and Y is *--S(O).sub.2CH.sub.2--. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heteroaryl, wherein said heteroaryl
comprises an endocyclic boron, and Y is *--NHC(O)OCH.sub.2--. In
this paragraph, * represents the point of attachment to Z.
[0130] In an exemplary embodiment, the compound is Formula (I), X
is as described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl has one ring, and said ring
comprises an endocyclic boron, and Y is substituted alkylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl has one ring, and said ring
comprises an endocyclic boron, and Y is unsubstituted alkylene. In
an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl has one ring, and said ring
comprises an endocyclic boron, and Y is methylene. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is substituted or unsubstituted heteroaryl, wherein said
heteroaryl has one ring, and said ring comprises an endocyclic
boron, and Y is ethylene. In an exemplary embodiment, the compound
is Formula (I), X is as described herein, W is H, Z is substituted
or unsubstituted heteroaryl, wherein said heteroaryl has one ring,
and said ring comprises an endocyclic boron, and Y is propylene. In
an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl has one ring, and said ring
comprises an endocyclic boron, and Y is substituted heteroalkylene.
In an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl has one ring, and said ring
comprises an endocyclic boron, and Y is unsubstituted
heteroalkylene. In an exemplary embodiment, the compound is Formula
(I), X is as described herein, W is H, Z is substituted or
unsubstituted heteroaryl, wherein said heteroaryl has one ring, and
said ring comprises an endocyclic boron, and Y is *--OCH.sub.2--.
In an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl has one ring, and said ring
comprises an endocyclic boron, and Y is *--SCH.sub.2--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl has one ring, and said ring
comprises an endocyclic boron, and Y is *--NHCH.sub.2--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl has one ring, and said ring
comprises an endocyclic boron, and Y is *--CH.sub.2NH--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl has one ring, and said ring
comprises an endocyclic boron, and Y is *--C(O)NH--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl has one ring, and said ring
comprises an endocyclic boron, and Y is *--CH.sub.2NHCH.sub.2-- or
1-piperazinyl or *--S(O)CH.sub.2-- or *--S(O).sub.2--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl has one ring, and said ring
comprises an endocyclic boron, and Y is 1-piperazinyl. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl has one ring, and said ring
comprises an endocyclic boron, and Y is *--S(O)CH.sub.2--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl has one ring, and said ring
comprises an endocyclic boron, and Y is *--S(O).sub.2--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl has one ring, and said ring
comprises an endocyclic boron, and Y is *--S(O).sub.2CH.sub.2--. In
an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl has one ring, and said ring
comprises an endocyclic boron, and Y is *--NHC(O)OCH.sub.2--. In
this paragraph, * represents the point of attachment to Z.
[0131] In an exemplary embodiment, the compound is Formula (I), X
is as described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl has two rings, and one of the
two rings comprises an endocyclic boron, and Y is substituted
alkylene. In an exemplary embodiment, the compound is Formula (I),
X is as described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl has two rings, and one of the
two rings comprises an endocyclic boron, and Y is unsubstituted
alkylene. In an exemplary embodiment, the compound is Formula (I),
X is as described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl has two rings, and one of the
two rings comprises an endocyclic boron, and Y is methylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl has two rings, and one of the
two rings comprises an endocyclic boron, and Y is ethylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl has two rings, and one of the
two rings comprises an endocyclic boron, and Y is propylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heteroaryl, wherein said heteroaryl has two rings, and one of the
two rings comprises an endocyclic boron, and Y is substituted
heteroalkylene. In an exemplary embodiment, the compound is Formula
(I), X is as described herein, W is H, Z is substituted or
unsubstituted heteroaryl, wherein said heteroaryl has two rings,
and one of the two rings comprises an endocyclic boron, and Y is
unsubstituted heteroalkylene. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heteroaryl, wherein said heteroaryl
has two rings, and one of the two rings comprises an endocyclic
boron, and Y is *--OCH.sub.2--. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heteroaryl, wherein said heteroaryl
has two rings, and one of the two rings comprises an endocyclic
boron, and Y is *--SCH.sub.2--. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heteroaryl, wherein said heteroaryl
has two rings, and one of the two rings comprises an endocyclic
boron, and Y is *--NHCH.sub.2--. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heteroaryl, wherein said heteroaryl
has two rings, and one of the two rings comprises an endocyclic
boron, and Y is *--CH.sub.2NH--. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heteroaryl, wherein said heteroaryl
has two rings, and one of the two rings comprises an endocyclic
boron, and Y is *--C(O)NH--. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heteroaryl, wherein said heteroaryl
has two rings, and one of the two rings comprises an endocyclic
boron, and Y is *--CH.sub.2NHCH.sub.2-- or 1-piperazinyl or
*--S(O)CH.sub.2-- or *--S(O).sub.2--. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heteroaryl, wherein said heteroaryl
has two rings, and one of the two rings comprises an endocyclic
boron, and Y is 1-piperazinyl. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heteroaryl, wherein said heteroaryl
has two rings, and one of the two rings comprises an endocyclic
boron, and Y is *--S(O)CH.sub.2--. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heteroaryl, wherein said heteroaryl
has two rings, and one of the two rings comprises an endocyclic
boron, and Y is *--S(O).sub.2--. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heteroaryl, wherein said heteroaryl
has two rings, and one of the two rings comprises an endocyclic
boron, and Y is *--S(O).sub.2CH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is substituted or unsubstituted heteroaryl, wherein said
heteroaryl has two rings, and one of the two rings comprises an
endocyclic boron, and Y is *--NHC(O)OCH.sub.2--. In this paragraph,
* represents the point of attachment to Z.
[0132] In an exemplary embodiment, the compound is Formula (I), X
is as described herein, W is H, Z is substituted or unsubstituted
heterocycloalkyl, wherein said heterocycloalkyl comprises an
endocyclic boron, and Y is substituted alkylene. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is substituted or unsubstituted heterocycloalkyl, wherein
said heterocycloalkyl comprises an endocyclic boron, and Y is
unsubstituted alkylene. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is substituted or
unsubstituted heterocycloalkyl, wherein said heterocycloalkyl
comprises an endocyclic boron, and Y is methylene. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is substituted or unsubstituted heterocycloalkyl, wherein
said heterocycloalkyl comprises an endocyclic boron, and Y is
ethylene. In an exemplary embodiment, the compound is Formula (I),
X is as described herein, W is H, Z is substituted or unsubstituted
heterocycloalkyl, wherein said heterocycloalkyl comprises an
endocyclic boron, and Y is propylene. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heterocycloalkyl, wherein said
heterocycloalkyl comprises an endocyclic boron, and Y is
substituted heteroalkylene. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heterocycloalkyl, wherein said
heterocycloalkyl comprises an endocyclic boron, and Y is
unsubstituted heteroalkylene. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heterocycloalkyl, wherein said
heterocycloalkyl comprises an endocyclic boron, and Y is
*--OCH.sub.2--. In an exemplary embodiment, the compound is Formula
(I), X is as described herein, W is H, Z is substituted or
unsubstituted heterocycloalkyl, wherein said heterocycloalkyl
comprises an endocyclic boron, and Y is *--SCH.sub.2--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heterocycloalkyl, wherein said heterocycloalkyl comprises an
endocyclic boron, and Y is *--NHCH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is substituted or unsubstituted heterocycloalkyl, wherein
said heterocycloalkyl comprises an endocyclic boron, and Y is
*--CH.sub.2NH--. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is substituted or
unsubstituted heterocycloalkyl, wherein said heterocycloalkyl
comprises an endocyclic boron, and Y is *--C(O)NH--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heterocycloalkyl, wherein said heterocycloalkyl comprises an
endocyclic boron, and Y is *--CH.sub.2NHCH.sub.2-- or 1-piperazinyl
or *--S(O)CH.sub.2-- or *--S(O).sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is substituted or unsubstituted heterocycloalkyl, wherein
said heterocycloalkyl comprises an endocyclic boron, and Y is
1-piperazinyl. In an exemplary embodiment, the compound is Formula
(I), X is as described herein, W is H, Z is substituted or
unsubstituted heterocycloalkyl, wherein said heterocycloalkyl
comprises an endocyclic boron, and Y is *--S(O)CH.sub.2--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heterocycloalkyl, wherein said heterocycloalkyl comprises an
endocyclic boron, and Y is *--S(O)-- In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heterocycloalkyl, wherein said
heterocycloalkyl comprises an endocyclic boron, and Y is
*--S(O).sub.2CH.sub.2--. In an exemplary embodiment, the compound
is Formula (I), X is as described herein, W is H, Z is substituted
or unsubstituted heterocycloalkyl, wherein said heterocycloalkyl
comprises an endocyclic boron, and Y is *--NHC(O)OCH.sub.2--. In
this paragraph, * represents the point of attachment to Z.
[0133] In an exemplary embodiment, the compound is Formula (I), X
is as described herein, W is H, Z is substituted or unsubstituted
heterocycloalkyl, wherein said heterocycloalkyl has one ring, and
said ring comprises an endocyclic boron, and Y is substituted
alkylene. In an exemplary embodiment, the compound is Formula (I),
X is as described herein, W is H, Z is substituted or unsubstituted
heterocycloalkyl, wherein said heterocycloalkyl has one ring, and
said ring comprises an endocyclic boron, and Y is unsubstituted
alkylene. In an exemplary embodiment, the compound is Formula (I),
X is as described herein, W is H, Z is substituted or unsubstituted
heterocycloalkyl, wherein said heterocycloalkyl has one ring, and
said ring comprises an endocyclic boron, and Y is methylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heterocycloalkyl, wherein said heterocycloalkyl has one ring, and
said ring comprises an endocyclic boron, and Y is ethylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heterocycloalkyl, wherein said heterocycloalkyl has one ring, and
said ring comprises an endocyclic boron, and Y is propylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heterocycloalkyl, wherein said heterocycloalkyl has one ring, and
said ring comprises an endocyclic boron, and Y is substituted
heteroalkylene. In an exemplary embodiment, the compound is Formula
(I), X is as described herein, W is H, Z is substituted or
unsubstituted heterocycloalkyl, wherein said heterocycloalkyl has
one ring, and said ring comprises an endocyclic boron, and Y is
unsubstituted heteroalkylene. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heterocycloalkyl, wherein said
heterocycloalkyl has one ring, and said ring comprises an
endocyclic boron, and Y is *--OCH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is substituted or unsubstituted heterocycloalkyl, wherein
said heterocycloalkyl has one ring, and said ring comprises an
endocyclic boron, and Y is *--SCH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is substituted or unsubstituted heterocycloalkyl, wherein
said heterocycloalkyl has one ring, and said ring comprises an
endocyclic boron, and Y is *--NHCH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is substituted or unsubstituted heterocycloalkyl, wherein
said heterocycloalkyl has one ring, and said ring comprises an
endocyclic boron, and Y is *--CH.sub.2NH--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is substituted or unsubstituted heterocycloalkyl, wherein
said heterocycloalkyl has one ring, and said ring comprises an
endocyclic boron, and Y is *--C(O)NH--. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heterocycloalkyl, wherein said
heterocycloalkyl has one ring, and said ring comprises an
endocyclic boron, and Y is *--CH.sub.2NHCH.sub.2- or 1-piperazinyl
or *--S(O)CH.sub.2-- or *--S(O).sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is substituted or unsubstituted heterocycloalkyl, wherein
said heterocycloalkyl has one ring, and said ring comprises an
endocyclic boron, and Y is 1-piperazinyl. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is substituted or unsubstituted heterocycloalkyl, wherein
said heterocycloalkyl has one ring, and said ring comprises an
endocyclic boron, and Y is *--S(O)CH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is substituted or unsubstituted heterocycloalkyl, wherein
said heterocycloalkyl has one ring, and said ring comprises an
endocyclic boron, and Y is *--S(O).sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is substituted or unsubstituted heterocycloalkyl, wherein
said heterocycloalkyl has one ring, and said ring comprises an
endocyclic boron, and Y is *--S(O).sub.2CH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is substituted or unsubstituted heterocycloalkyl, wherein
said heterocycloalkyl has one ring, and said ring comprises an
endocyclic boron, and Y is *--NHC(O)OCH.sub.2--. In this paragraph,
* represents the point of attachment to Z.
[0134] In an exemplary embodiment, the compound is Formula (I), X
is as described herein, W is H, Z is substituted or unsubstituted
heterocycloalkyl, wherein said heterocycloalkyl has two rings, and
one of the two rings comprises an endocyclic boron, and Y is
substituted alkylene. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is substituted or
unsubstituted heterocycloalkyl, wherein said heterocycloalkyl has
two rings, and one of the two rings comprises an endocyclic boron,
and Y is unsubstituted alkylene. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heterocycloalkyl, wherein said
heterocycloalkyl has two rings, and one of the two rings comprises
an endocyclic boron, and Y is methylene. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is substituted or unsubstituted heterocycloalkyl, wherein
said heterocycloalkyl has two rings, and one of the two rings
comprises an endocyclic boron, and Y is ethylene. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is substituted or unsubstituted heterocycloalkyl, wherein
said heterocycloalkyl has two rings, and one of the two rings
comprises an endocyclic boron, and Y is propylene. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is substituted or unsubstituted heterocycloalkyl, wherein
said heterocycloalkyl has two rings, and one of the two rings
comprises an endocyclic boron, and Y is substituted heteroalkylene.
In an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heterocycloalkyl, wherein said heterocycloalkyl has two rings, and
one of the two rings comprises an endocyclic boron, and Y is
unsubstituted heteroalkylene. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heterocycloalkyl, wherein said
heterocycloalkyl has two rings, and one of the two rings comprises
an endocyclic boron, and Y is *--OCH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is substituted or unsubstituted heterocycloalkyl, wherein
said heterocycloalkyl has two rings, and one of the two rings
comprises an endocyclic boron, and Y is *--SCH.sub.2--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heterocycloalkyl, wherein said heterocycloalkyl has two rings, and
one of the two rings comprises an endocyclic boron, and Y is
*--NHCH.sub.2--. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is substituted or
unsubstituted heterocycloalkyl, wherein said heterocycloalkyl has
two rings, and one of the two rings comprises an endocyclic boron,
and Y is *--CH.sub.2NH--. In an exemplary embodiment, the compound
is Formula (I), X is as described herein, W is H, Z is substituted
or unsubstituted heterocycloalkyl, wherein said heterocycloalkyl
has two rings, and one of the two rings comprises an endocyclic
boron, and Y is *--C(O)NH--. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heterocycloalkyl, wherein said
heterocycloalkyl has two rings, and one of the two rings comprises
an endocyclic boron, and Y is *--CH.sub.2NHCH.sub.2-- or
1-piperazinyl or *--S(O)CH.sub.2-- or *--S(O).sub.2--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heterocycloalkyl, wherein said heterocycloalkyl has two rings, and
one of the two rings comprises an endocyclic boron, and Y is
1-piperazinyl. In an exemplary embodiment, the compound is Formula
(I), X is as described herein, W is H, Z is substituted or
unsubstituted heterocycloalkyl, wherein said heterocycloalkyl has
two rings, and one of the two rings comprises an endocyclic boron,
and Y is *--S(O)CH.sub.2--. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is
substituted or unsubstituted heterocycloalkyl, wherein said
heterocycloalkyl has two rings, and one of the two rings comprises
an endocyclic boron, and Y is *--S(O).sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is substituted or unsubstituted heterocycloalkyl, wherein
said heterocycloalkyl has two rings, and one of the two rings
comprises an endocyclic boron, and Y is *--S(O).sub.2CH.sub.2--. In
an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is substituted or unsubstituted
heterocycloalkyl, wherein said heterocycloalkyl has two rings, and
one of the two rings comprises an endocyclic boron, and Y is
*--NHC(O)OCH.sub.2--. In this paragraph, * represents the point of
attachment to Z.
[0135] In an exemplary embodiment, the compound is Formula (I), X
is as described herein, W is H, Z is a benzoxaborole described
herein, and Y is substituted alkylene. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
a benzoxaborole described herein, and Y is unsubstituted alkylene.
In an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a benzoxaborole described herein,
and Y is methylene. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is a benzoxaborole
described herein, and Y is ethylene. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
a benzoxaborole described herein, and Y is propylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a benzoxaborole described herein,
and Y is substituted heteroalkylene. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
a benzoxaborole described herein, and Y is unsubstituted
heteroalkylene. In an exemplary embodiment, the compound is Formula
(I), X is as described herein, W is H, Z is a benzoxaborole
described herein, and Y is *--OCH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is a benzoxaborole described herein, and Y is
*--SCH.sub.2--. In an exemplary embodiment, the compound is Formula
(I), X is as described herein, W is H, Z is a benzoxaborole
described herein, and Y is *--NHCH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is a benzoxaborole described herein, and Y is
*--CH.sub.2NH--. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is a benzoxaborole
described herein, and Y is *--C(O)NH--. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
a benzoxaborole described herein, and Y is *--CH.sub.2NHCH.sub.2--
or 1-piperazinyl or *--S(O)CH.sub.2-- or *--S(O).sub.2--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a benzoxaborole described herein,
and Y is 1-piperazinyl. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is a benzoxaborole
described herein, and Y is *--S(O)CH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is a benzoxaborole described herein, and Y is
*--S(O).sub.2--. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is a benzoxaborole
described herein, and Y is *--S(O).sub.2CH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is a benzoxaborole described herein, and Y is
*--NHC(O)OCH.sub.2--. In this paragraph, * represents the point of
attachment to Z.
[0136] In an exemplary embodiment, the compound is Formula (I), X
is as described herein, W is H, Z is Formula (II), R.sup.3 is H,
R.sup.3a is H, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is H, and Y
is substituted alkylene. In an exemplary embodiment, the compound
is Formula (I), X is as described herein, W is H, Z is Formula
(II), R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.5 is H, and
R.sup.7 is H, and Y is unsubstituted alkylene. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is Formula (II), R.sup.3 is H, R.sup.3a is H, R.sup.4 is
H, R.sup.5 is H, and R.sup.7 is H, and Y is methylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is Formula (II), R.sup.3 is H, R.sup.3a
is H, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is H, and Y is
ethylene. In an exemplary embodiment, the compound is Formula (I),
X is as described herein, W is H, Z is Formula (II), R.sup.3 is H,
R.sup.3a is H, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is H, and Y
is propylene. In an exemplary embodiment, the compound is Formula
(I), X is as described herein, W is H, Z is Formula (II), R.sup.3
is H, R.sup.3a is H, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is H,
and Y is substituted heteroalkylene. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
Formula (II), R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.5 is
H, and R.sup.7 is H, and Y is unsubstituted heteroalkylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is Formula (II), R.sup.3 is H, R.sup.3a
is H, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is H, and Y is
*--OCH.sub.2--. In an exemplary embodiment, the compound is Formula
(I), X is as described herein, W is H, Z is Formula (II), R.sup.3
is H, R.sup.3a is H, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is H,
and Y is *--SCH.sub.2--. In an exemplary embodiment, the compound
is Formula (I), X is as described herein, W is H, Z is Formula
(II), R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.5 is H, and
R.sup.7 is H, and Y is *--NHCH.sub.2--. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
Formula (II), R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.5 is
H, and R.sup.7 is H, and Y is *--CH.sub.2NH--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is Formula (II), R.sup.3 is H, R.sup.3a is H, R.sup.4 is
H, R.sup.5 is H, and R.sup.7 is H, and Y is *--C(O)NH--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is Formula (II), R.sup.3 is H, R.sup.3a
is H, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is H, and Y is
*--CH.sub.2NHCH.sub.2- or 1-piperazinyl or *--S(O)CH.sub.2-- or
*--S(O).sub.2--. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is Formula (II),
R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.5 is H, and
R.sup.7 is H, and Y is 1-piperazinyl. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
Formula (II), R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.5 is
H, and R.sup.7 is H, and Y is *--S(O)CH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is Formula (II), R.sup.3 is H, R.sup.3a is H, R.sup.4 is
H, R.sup.5 islH, and R.sup.7 is H, and Y is *--S(O).sub.2--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is Formula (II), R.sup.3 is H, R.sup.3a
is H, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is H, and Y is
*--S(O).sub.2CH.sub.2--. In an exemplary embodiment, the compound
is Formula (I), X is as described herein, W is H, Z is Formula
(II), R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.5 is H, and
R.sup.7 is H, and Y is *--NHC(O)OCH.sub.2--. In this paragraph, *
represents the point of attachment to Z.
[0137] In an exemplary embodiment, the compound is Formula (I), X
is as described herein, W is H, Z is Formula (III), R.sup.3 is H,
R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and R.sup.7 is H, and Y
is substituted alkylene. In an exemplary embodiment, the compound
is Formula (I), X is as described herein, W is H, Z is Formula
(III), R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and
R.sup.7 is H, and Y is unsubstituted alkylene. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is Formula (III), R.sup.3 is H, R.sup.3a is H, R.sup.4 is
H, R.sup.6 is H, and R.sup.7 is H, and Y is methylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is Formula (III), R.sup.3 is H,
R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and R.sup.7 is H, and Y
is ethylene. In an exemplary embodiment, the compound is Formula
(I), X is as described herein, W is H, Z is Formula (III), R.sup.3
is H, R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and R.sup.7 is H,
and Y is propylene. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is Formula (III),
R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and
R.sup.7 is H, and Y is substituted heteroalkylene. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is Formula (III), R.sup.3 is H, R.sup.3a is H, R.sup.4 is
H, R.sup.6 is H, and R.sup.7 is H, and Y is unsubstituted
heteroalkylene. In an exemplary embodiment, the compound is Formula
(I), X is as described herein, W is H, Z is Formula (III), R.sup.3
is H, R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and R.sup.7 is H,
and Y is *--OCH.sub.2--. In an exemplary embodiment, the compound
is Formula (I), X is as described herein, W is H, Z is Formula
(III), R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and
R.sup.7 is H, and Y is *--SCH.sub.2--. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
Formula (III), R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.6
is H, and R.sup.7 is H, and Y is *--NHCH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is Formula (III), R.sup.3 is H, R.sup.3a is H, R.sup.4 is
H, R.sup.6 is H, and R.sup.7 is H, and Y is *--CH.sub.2NH--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is Formula (III), R.sup.3 is H,
R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and R.sup.7 is H, and Y
is *--C(O)NH--. In an exemplary embodiment, the compound is Formula
(I), X is as described herein, W is H, Z is Formula (III), R.sup.3
is H, R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and R.sup.7 is H,
and Y is *--CH.sub.2NHCH.sub.2-- or 1-piperazinyl or
*--S(O)CH.sub.2-- or *--S(O).sub.2--. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
Formula (III), R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.6
is H, and R.sup.7 is H, and Y is 1-piperazinyl. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is Formula (III), R.sup.3 is H, R.sup.3a is H, R.sup.4 is
H, R.sup.6 is H, and R.sup.7 is H, and Y is *--S(O)CH.sub.2--. In
an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is Formula (III), R.sup.3 is H,
R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and R.sup.7 is H, and Y
is *--S(O).sub.2--. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is Formula (III),
R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and
R.sup.7 is H, and Y is *--S(o).sub.2CH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is Formula (III), R.sup.3 is H, R.sup.3a is H, R.sup.4 is
H, R.sup.6 is H, and R.sup.7 is H, and Y is *--NHC(O)OCH.sub.2--.
In this paragraph, * represents the point of attachment to Z.
[0138] In an exemplary embodiment, the compound is Formula (I), X
is as described herein, W is H, Z is Formula (II), R.sup.3 is H,
R.sup.3a is H, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is F, and Y
is substituted alkylene. In an exemplary embodiment, the compound
is Formula (I), X is as described herein, W is H, Z is Formula
(II), R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.5 is H, and
R.sup.7 is F, and Y is unsubstituted alkylene. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is Formula (II), R.sup.3 is H, R.sup.3a is H, R.sup.4 is
H, R.sup.5 is H, and R.sup.7 is F, and Y is methylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is Formula (II), R.sup.3 is H, R.sup.3a
is H, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is F, and Y is
ethylene. In an exemplary embodiment, the compound is Formula (I),
X is as described herein, W is H, Z is Formula (II), R.sup.3 is H,
R.sup.3a is H, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is F, and Y
is propylene. In an exemplary embodiment, the compound is Formula
(I), X is as described herein, W is H, Z is Formula (II), R.sup.3
is H, R.sup.3a is H, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is F,
and Y is substituted heteroalkylene. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
Formula (II), R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.5 is
H, and R.sup.7 is F, and Y is unsubstituted heteroalkylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is Formula (II), R.sup.3 is H, R.sup.3a
is H, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is F, and Y is
*--OCH.sub.2--. In an exemplary embodiment, the compound is Formula
(I), X is as described herein, W is H, Z is Formula (II), R.sup.3
is H, R.sup.3a is H, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is F,
and Y is *--SCH.sub.2--. In an exemplary embodiment, the compound
is Formula (I), X is as described herein, W is H, Z is Formula
(II), R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.5 is H, and
R.sup.7 is F, and Y is *--NHCH.sub.2--. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
Formula (II), R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.5 is
H, and R.sup.7 is F, and Y is *--CH.sub.2NH--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is Formula (II), R.sup.3 is H, R.sup.3a is H, R.sup.4 is
H, R.sup.5 is H, and R.sup.7 is F, and Y is *--C(O)NH--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is Formula (II), R.sup.3 is H, R.sup.3a
is H, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is F, and Y is
*--CH.sub.2NHCH.sub.2- or 1-piperazinyl or *--S(O)CH.sub.2-- or
*--S(O).sub.2--. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is Formula (II),
R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.5 is H, and
R.sup.7 is F, and Y is 1-piperazinyl. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
Formula (II), R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.5 is
H, and R.sup.7 is F, and Y is *--S(O)CH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is Formula (II), R.sup.3 is H, R.sup.3a is H, R.sup.4 is
H, R.sup.5 is H, and R.sup.7 is F, and Y is *--S(O).sub.2--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is Formula (II), R.sup.3 is H, R.sup.3a
is H, R.sup.4 is H, R.sup.5 is H, and R.sup.7 is F, and Y is
*--S(O).sub.2CH.sub.2--. In an exemplary embodiment, the compound
is Formula (I), X is as described herein, W is H, Z is Formula
(II), R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.5 is H, and
R.sup.7 is F, and Y is *--NHC(O)OCH.sub.2--. In this paragraph, *
represents the point of attachment to Z.
[0139] In an exemplary embodiment, the compound is Formula (I), X
is as described herein, W is H, Z is Formula (III), R.sup.3 is H,
R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and R.sup.7 is F, and Y
is substituted alkylene. In an exemplary embodiment, the compound
is Formula (I), X is as described herein, W is H, Z is Formula
(III), R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and
R.sup.7 is F, and Y is unsubstituted alkylene. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is Formula (III), R.sup.3 is H, R.sup.3a is H, R.sup.4 is
H, R.sup.6 is H, and R.sup.7 is F, and Y is methylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is Formula (III), R.sup.3 is H,
R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and R.sup.7 is F, and Y
is ethylene. In an exemplary embodiment, the compound is Formula
(I), X is as described herein, W is H, Z is Formula (III), R.sup.3
is H, R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and R.sup.7 is F,
and Y is propylene. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is Formula (III),
R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and
R.sup.7 is F, and Y is substituted heteroalkylene. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is Formula (III), R.sup.3 is H, R.sup.3a is H, R.sup.4 is
H, R.sup.6 is H, and R.sup.7 is F, and Y is unsubstituted
heteroalkylene. In an exemplary embodiment, the compound is Formula
(I), X is as described herein, W is H, Z is Formula (III), R.sup.3
is H, R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and R.sup.7 is F,
and Y is *--OCH.sub.2--. In an exemplary embodiment, the compound
is Formula (I), X is as described herein, W is H, Z is Formula
(III), R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and
R.sup.7 is F, and Y is *--SCH.sub.2--. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
Formula (III), R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.6
is H, and R.sup.7 is F, and Y is *--NHCH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is Formula (III), R.sup.3 is H, R.sup.3a is H, R.sup.4 is
H, R.sup.6 is H, and R.sup.7 is F, and Y is *--CH.sub.2NH--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is Formula (III), R.sup.3 is H,
R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and R.sup.7 is F, and Y
is *--C(O)NH--. In an exemplary embodiment, the compound is Formula
(I), X is as described herein, W is H, Z is Formula (III), R.sup.3
is H, R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and R.sup.7 is F,
and Y is *--CH.sub.2NHCH.sub.2- or 1-piperazinyl or
*--S(O)CH.sub.2-- or *--S(O).sub.2--. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
Formula (III), R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.6
is H, and R.sup.7 is F, and Y is 1-piperazinyl. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is Formula (III), R.sup.3 is H, R.sup.3a is H, R.sup.4 is
H, R.sup.6 is H, and R.sup.7 is F, and Y is *--S(O)CH.sub.2--. In
an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is Formula (III), R.sup.3 is H,
R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and R.sup.7 is F, and Y
is *--S(O).sub.2--. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is Formula (III),
R.sup.3 is H, R.sup.3a is H, R.sup.4 is H, R.sup.6 is H, and
R.sup.7 is F, and Y is *--S(O).sub.2CH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is Formula (III), R.sup.3 is H, R.sup.3a is H, R.sup.4 is
H, R.sup.6 is H, and R.sup.7 is F, and Y is *--NHC(O)OCH.sub.2--.
In this paragraph, * represents the point of attachment to Z.
[0140] In an exemplary embodiment, the compound is Formula (I), X
is as described herein, W is H, Z is a pyridinyloxaborole described
herein, and Y is substituted alkylene. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
a pyridinyloxaborole described herein, and Y is unsubstituted
alkylene. In an exemplary embodiment, the compound is Formula (I),
X is as described herein, W is H, Z is a pyridinyloxaborole
described herein, and Y is methylene. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
a pyridinyloxaborole described herein, and Y is ethylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a pyridinyloxaborol described
herein, and Y is propylene. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is a
pyridinyloxaborole described herein, and Y is substituted
heteroalkylene. In an exemplary embodiment, the compound is Formula
(I), X is as described herein, W is H, Z is a pyridinyloxaborole
described herein, and Y is unsubstituted heteroalkylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a pyridinyloxaborole described
herein, and Y is *--OCH.sub.2--. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is a
pyridinyloxaborole described herein, and Y is *--SCH.sub.2--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a pyridinyloxaborole described
herein, and Y is *--NHCH.sub.2--. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is a
pyridinyloxaborole described herein, and Y is *--CH.sub.2NH--. In
an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a pyridinyloxaborole described
herein, and Y is *--C(O)NH--. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is a
pyridinyloxaborole described herein, and Y is
*--CH.sub.2NHCH.sub.2-- or 1-piperazinyl or *--S(O)CH.sub.2-- or
*--S(O).sub.2--. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is a
pyridinyloxaborole described herein, and Y is 1-piperazinyl. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a pyridinyloxaborole described
herein, and Y is *--S(O)CH.sub.2--. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is a
pyridinyloxaborole described herein, and Y is *--S(O).sub.2--. In
an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a pyridinyloxaborole described
herein, and Y is *--S(o).sub.2CH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is a pyridinyloxaborole described herein, and Y is
*--NHC(O)OCH.sub.2--. In this paragraph, * represents the point of
attachment to Z.
[0141] In an exemplary embodiment, the compound is Formula (I), X
is as described herein, W is H, Z is a benzoxaborininol described
herein, and Y is substituted alkylene. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
a benzoxaborininol described herein, and Y is unsubstituted
alkylene. In an exemplary embodiment, the compound is Formula (I),
X is as described herein, W is H, Z is a benzoxaborininol described
herein, and Y is methylene. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is a
benzoxaborininol described herein, and Y is ethylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a benzoxaborininol described herein,
and Y is propylene. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is a
benzoxaborininol described herein, and Y is substituted
heteroalkylene. In an exemplary embodiment, the compound is Formula
(I), X is as described herein, W is H, Z is abenzoxaborininol
described herein, and Y is unsubstituted heteroalkylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a benzoxaborininol described herein,
and Y is *--OCH.sub.2--. In an exemplary embodiment, the compound
is Formula (I), X is as described herein, W is H, Z is a
benzoxaborininol described herein, and Y is *--SCH.sub.2--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a benzoxaborininol described herein,
and Y is *--NHCH.sub.2--. In an exemplary embodiment, the compound
is Formula (I), X is as described herein, W is H, Z is a
benzoxaborininol described herein, and Y is *--CH.sub.2NH--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a benzoxaborininol described herein,
and Y is *--C(O)NH--. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is a
benzoxaborininol described herein, and Y is *--CH.sub.2NHCH.sub.2--
or 1-piperazinyl or *--S(O)CH.sub.2-- or *--S(O).sub.2--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a benzoxaborininol described herein,
and Y is 1-piperazinyl. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is a
benzoxaborininol described herein, and Y is *--S(O)CH.sub.2--. In
an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a benzoxaborininol described herein,
and Y is *--S(O).sub.2--. In an exemplary embodiment, the compound
is Formula (I), X is as described herein, W is H, Z is a
benzoxaborininol described herein, and Y is
*--S(O).sub.2CH.sub.2--. In an exemplary embodiment, the compound
is Formula (I), X is as described herein, W is H, Z is a
benzoxaborininol described herein, and Y is *--NHC(O)OCH.sub.2--.
In this paragraph, * represents the point of attachment to Z.
[0142] In an exemplary embodiment, the compound is Formula (I), X
is as described herein, W is H, Z is a benzoxazaborininol described
herein, and Y is substituted alkylene. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
a benzoxazaborininol described herein, and Y is unsubstituted
alkylene. In an exemplary embodiment, the compound is Formula (I),
X is as described herein, W is H, Z is a benzoxazaborininol
described herein, and Y is methylene. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
a benzoxazaborininol described herein, and Y is ethylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a benzoxazaborininol described
herein, and Y is propylene. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is a
benzoxazaborininol described herein, and Y is substituted
heteroalkylene. In an exemplary embodiment, the compound is Formula
(I), X is as described herein, W is H, Z is a benzoxazaborininol
described herein, and Y is unsubstituted heteroalkylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a benzoxazaborininol described
herein, and Y is *--OCH.sub.2--. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is a
benzoxazaborininol described herein, and Y is *--SCH.sub.2--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a benzoxazaborininol described
herein, and Y is *-NHCH.sub.2-. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is a
benzoxazaborininol described herein, and Y is *--CH.sub.2NH--. In
an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a benzoxazaborininol described
herein, and Y is *--C(O)NH--. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is a
benzoxazaborininol described herein, and Y is
*--CH.sub.2NHCH.sub.2-- or 1-piperazinyl or *--S(O)CH.sub.2-- or
*--S(O).sub.2--. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is a
benzoxazaborininol described herein, and Y is 1-piperazinyl. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a benzoxazaborininol described
herein, and Y is *--S(O)CH.sub.2--. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is a
benzoxazaborininol described herein, and Y is *--S(O).sub.2--. In
an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a benzoxazaborininol described
herein, and Y is *--S(o).sub.2CH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is a benzoxazaborininol described herein, and Y is
*--NHC(O)OCH.sub.2--. In this paragraph, * represents the point of
attachment to Z.
[0143] In an exemplary embodiment, the compound is Formula (I), X
is as described herein, W is H, Z is a benzodiazaborininol
described herein, and Y is substituted alkylene. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is a benzodiazaborininol described herein, and Y is
unsubstituted alkylene. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is a
benzodiazaborininol described herein, and Y is methylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a benzodiazaborininol described
herein, and Y is ethylene. In an exemplary embodiment, the compound
is Formula (I), X is as described herein, W is H, Z is a
benzodiazaborininol described herein, and Y is propylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a benzodiazaborininol described
herein, and Y is substituted heteroalkylene. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is a benzodiazaborininol described herein, and Y is
unsubstituted heteroalkylene. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is a
benzodiazaborininol described herein, and Y is *--OCH.sub.2--. In
an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a benzodiazaborininol described
herein, and Y is *--SCH.sub.2--. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is a
benzodiazaborininol described herein, and Y is *--NHCH.sub.2--. In
an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a benzodiazaborininol described
herein, and Y is *--CH.sub.2NH--. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is a
benzodiazaborininol described herein, and Y is *--C(O)NH--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a benzodiazaborininol described
herein, and Y is *--CH.sub.2NHCH.sub.2-- or 1-piperazinyl or
*--S(O)CH.sub.2-- or *--S(O).sub.2--. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
a benzodiazaborininol described herein, and Y is 1-piperazinyl. In
an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a benzodiazaborininol described
herein, and Y is *--S(O)CH.sub.2--. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is a
benzodiazaborininol described herein, and Y is *--S(O).sub.2--. In
an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a benzodiazaborininol described
herein, and Y is *--S(O).sub.2CH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is a benzodiazaborininol described herein, and Y is
*--NHC(O)OCH.sub.2--. In this paragraph, * represents the point of
attachment to Z.
[0144] In an exemplary embodiment, the compound is Formula (I), X
is as described herein, W is H, Z is an oxaborole described herein,
and Y is substituted alkylene. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is an
oxaborole described herein, and Y is unsubstituted alkylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is an oxaborole described herein, and Y
is methylene. In an exemplary embodiment, the compound is Formula
(I), X is as described herein, W is H, Z is an oxaborole described
herein, and Y is ethylene. In an exemplary embodiment, the compound
is Formula (I), X is as described herein, W is H, Z is an oxaborole
described herein, and Y is propylene. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
an oxaborole described herein, and Y is substituted heteroalkylene.
In an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is an oxaborole described herein, and Y
is unsubstituted heteroalkylene. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is an
oxaborole described herein, and Y is *--OCH.sub.2--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is an oxaborole described herein, and Y
is *--SCH.sub.2--. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is an oxaborole
described herein, and Y is *--NHCH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is an oxaborole described herein, and Y is
*--CH.sub.2NH--. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is an oxaborole
described herein, and Y is *--C(O)NH--. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
an oxaborole described herein, and Y is *--CH.sub.2NHCH.sub.2-- or
1-piperazinyl or *--S(O)CH.sub.2-- or *--S(O).sub.2--. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is an oxaborole described herein, and Y
is 1-piperazinyl. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is an oxaborole
described herein, and Y is *--S(O)CH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is an oxaborole described herein, and Y is
*--S(O).sub.2--. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is an oxaborole
described herein, and Y is *--S(O).sub.2CH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is an oxaborole described herein, and Y is
*--NHC(O)OCH.sub.2--. In this paragraph, * represents the point of
attachment to Z.
[0145] In an exemplary embodiment, the compound is Formula (I), X
is as described herein, W is H, Z is a dihydrobenzoazaborinine
described herein, and Y is substituted alkylene. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is a dihydrobenzoazaborinine described herein, and Y is
unsubstituted alkylene. In an exemplary embodiment, the compound is
Formula (I), X is as described herein, W is H, Z is a
dihydrobenzoazaborinine described herein, and Y is methylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a dihydrobenzoazaborinine described
herein, and Y is ethylene. In an exemplary embodiment, the compound
is Formula (I), X is as described herein, W is H, Z is a
dihydrobenzoazaborinine described herein, and Y is propylene. In an
exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a dihydrobenzoazaborinine described
herein, and Y is substituted heteroalkylene. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is a dihydrobenzoazaborinine described herein, and Y is
unsubstituted heteroalkylene. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is a
dihydrobenzoazaborinine described herein, and Y is *--OCH.sub.2--.
In an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a dihydrobenzoazaborinine described
herein, and Y is *--SCH.sub.2--. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is a
dihydrobenzoazaborinine described herein, and Y is *--NHCH.sub.2--.
In an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a dihydrobenzoazaborinine described
herein, and Y is *--CH.sub.2NH--. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is a
dihydrobenzoazaborinine described herein, and Y is *--C(O)NH--. In
an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a dihydrobenzoazaborinine described
herein, and Y is *--CH.sub.2NHCH.sub.2-- or 1-piperazinyl or
*--S(O)CH.sub.2-- or *--S(O).sub.2--. In an exemplary embodiment,
the compound is Formula (I), X is as described herein, W is H, Z is
a dihydrobenzoazaborinine described herein, and Y is 1-piperazinyl.
In an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a dihydrobenzoazaborinine described
herein, and Y is *--S(O)CH.sub.2--. In an exemplary embodiment, the
compound is Formula (I), X is as described herein, W is H, Z is a
dihydrobenzoazaborinine described herein, and Y is *--S(O).sub.2--.
In an exemplary embodiment, the compound is Formula (I), X is as
described herein, W is H, Z is a dihydrobenzoazaborinine described
herein, and Y is *--S(O).sub.2CH.sub.2--. In an exemplary
embodiment, the compound is Formula (I), X is as described herein,
W is H, Z is a dihydrobenzoazaborinine described herein, and Y is
*--NHC(O)OCH.sub.2--. In this paragraph, * represents the point of
attachment to Z.
[0146] The compounds of the invention can form a hydrate with
water, solvates with alcohols such as methanol, ethanol, propanol,
and the like; adducts with amino compounds, such as ammonia,
methylamine, ethylamine, and the like; adducts with acids, such as
formic acid, acetic acid and the like; complexes with ethanolamine,
quinoline, amino acids, and the like.
[0147] In an exemplary embodiment, the invention provides a
compound described herein, or a salt, hydrate or solvate thereof,
or a combination thereof. In an exemplary embodiment, the invention
provides a compound described herein, or a salt, hydrate or solvate
thereof. In an exemplary embodiment, the invention provides a
compound described herein, or a salt thereof. In an exemplary
embodiment, the salt is a pharmaceutically acceptable salt. In an
exemplary embodiment, the invention provides a compound described
herein, or a hydrate thereof. In an exemplary embodiment, the
invention provides a compound described herein, or a solvate
thereof. In an exemplary embodiment, the invention provides a
compound described herein, or a prodrug thereof. In an exemplary
embodiment, the invention provides a salt of a compound described
herein. In an exemplary embodiment, the invention provides a
pharmaceutically acceptable salt of a compound described herein. In
an exemplary embodiment, the invention provides a hydrate of a
compound described herein. In an exemplary embodiment, the
invention provides a solvate of a compound described herein. In an
exemplary embodiment, the invention provides a prodrug of a
compound described herein.
[0148] In an exemplary embodiment, alkyl is linear alkyl. In
another exemplary embodiment, alkyl is branched alkyl.
[0149] In an exemplary embodiment, heteroalkyl is linear
heteroalkyl. In another exemplary embodiment, heteroalkyl is
branched heteroalkyl.
III. b) Combinations Comprising Additional Therapeutically Active
Agents
[0150] The compounds of the invention may also be used in
combination with at least one other therapeutically active agent.
The invention thus provides, in a further aspect, a combination
comprising a compound of the invention together with at least one
other therapeutically active agent, or a salt, prodrug, hydrate or
solvate thereof. In an exemplary embodiment, the compound of the
invention is a compound described herein, or a salt thereof. In an
exemplary embodiment, the additional therapeutically active agent
is a compound of the invention. In an exemplary embodiment, the
additional therapeutic agent includes a boron atom. In an exemplary
embodiment, the additional therapeutic agent does not contain a
boron atom. In an exemplary embodiment, the additional therapeutic
agent is a compound described in section III a).
[0151] When a compound of the invention is used in combination with
a second therapeutic agent active against the same disease state,
the dose of each compound may differ from that when the compound is
used alone. Appropriate doses will be readily appreciated by those
skilled in the art. It will be appreciated that the amount of a
compound of the invention required for use in treatment will vary
with the nature of the condition being treated and the age and the
condition of the patient and will be ultimately at the discretion
of the attendant physician or veterinarian.
[0152] The individual components of such combinations may be
administered either simultaneously or sequentially in a unit dosage
form. The unit dosage form may be a single or multiple unit dosage
forms. In an exemplary embodiment, the invention provides a
combination in a single unit dosage form. An example of a single
unit dosage form is a capsule wherein both the compound of the
invention and the additional therapeutic agent are contained within
the same capsule. In an exemplary embodiment, the invention
provides a combination in a two unit dosage form. An example of a
two unit dosage form is a first capsule which contains the compound
of the invention and a second capsule which contains the additional
therapeutic agent. Thus the term `single unit` or `two unit` or
`multiple unit` refers to the object which the animal (for example,
a human) ingests, not to the interior components of the object.
Appropriate doses of known therapeutic agents will be readily
appreciated by those skilled in the art.
[0153] The combinations referred to herein may conveniently be
presented for use in the form of a pharmaceutical formulation.
Thus, an exemplary embodiment of the invention is a pharmaceutical
formulation comprising a) a compound of the invention; b) an
additional therapeutic agent and c) a pharmaceutically acceptable
excipient. In an exemplary embodiment, the pharmaceutical
formulation is a unit dosage form. In an exemplary embodiment, the
pharmaceutical formulation is a single unit dosage form. In an
exemplary embodiment, the pharmaceutical formulation is a single
unit dosage form which includes a compound of the invention; an
antibacterial and a pharmaceutically acceptable excipient. In an
exemplary embodiment, the pharmaceutical formulation is a single
unit dosage form which includes a compound of the invention; an
antibacterial and at least one pharmaceutically acceptable
excipient. In an exemplary embodiment, the pharmaceutical
formulation is a two unit dosage form. In an exemplary embodiment,
the pharmaceutical formulation is a two unit dosage form comprising
a first unit dosage form and a second unit dosage form, wherein the
first unit dosage form includes a) a compound of the invention and
b) a first pharmaceutically acceptable excipient; and the second
unit dosage form includes c) an additional therapeutic agent and d)
a second pharmaceutically acceptable excipient. In an exemplary
embodiment, the pharmaceutical formulation is a two unit dosage
form comprising a first unit dosage form and a second unit dosage
form, wherein the first unit dosage form includes a) a compound of
the invention and b) a first pharmaceutically acceptable excipient;
and the second unit dosage form includes c) an antibacterial and d)
a second pharmaceutically acceptable excipient.
III. c) Preparation of Compounds of the Invention
[0154] Compounds of the invention can be prepared using
commercially available starting materials, known intermediates, or
by using the synthetic methods published in references described
and incorporated by reference herein, such as U.S. patent
application Ser. No. 12/142,692 and U.S. Pat. Pubs. US20060234981,
US20070155699 and US20070293457.
[0155] The following general procedures were used as indicated in
generating the examples and can be applied, using the knowledge of
one of skill in the art, to other appropriate compounds to obtain
additional analogues. Benzoxaborole, benzoxaborininol, and
benzodiazaborininol are shown below for exemplary purposes. The
procedures are adaptable to any of the boron ring systems described
herein.
General Procedures for Creating Modified Pleuromutilins:
[0156] A general method of creating a modified pleuromutilin is
provided below:
##STR00094##
[0157] Another general method of creating a modified pleuromutilin
is provided below:
##STR00095##
General Procedures for Attaching Modified Pleuromutilins to a Ring
System Containing at Least One Endocyclic Boron:
[0158] A general method of attaching a modified pleuromutilin to a
ring system containing at least one endocyclic boron is provided
below.
##STR00096##
[0159] Another general method of attaching a modified pleuromutilin
to a ring system containing at least one endocyclic boron is
provided below.
##STR00097##
[0160] Another general method of attaching a modified pleuromutilin
to a ring system containing at least one endocyclic boron is
provided below.
##STR00098##
[0161] Another general method of attaching a modified pleuromutilin
to a ring system containing at least one endocyclic boron is
provided below.
##STR00099##
[0162] Another general method of attaching a modified pleuromutilin
to a ring system containing at least one endocyclic boron is
provided below.
##STR00100##
[0163] Another general method of attaching a modified pleuromutilin
to a ring system containing at least one endocyclic boron is
provided below.
##STR00101##
General Procedures for Modifying a Pleuromutilin Containing a Ring
System with at Least One Endocyclic Boron:
[0164] A general method of modifying a pleuromutilin containing a
ring system with at least one endocyclic boron is provided
below:
##STR00102##
[0165] Another general method of modifying a pleuromutilin
containing a ring system with at least one endocyclic boron is
provided below:
##STR00103##
[0166] Another general method of modifying a pleuromutilin
containing a ring system with at least one endocyclic boron is
provided below:
##STR00104##
[0167] Another general method of modifying a pleuromutilin
containing a ring system with at least one endocyclic boron is
provided below:
##STR00105##
IV. Methods
[0168] In another aspect, the compounds of the invention and/or
combinations of the invention can be utilized to inhibit protein
synthesis in a bacteria. In another aspect, the compounds of the
invention and/or combinations of the invention exhibit potency
against microorganisms, such as bacteria, and worms, and therefore
have the potential to kill and/or inhibit the growth of them. In
another aspect, the compounds of the invention and/or combinations
of the invention exhibit potency against microorganisms, such as
bacteria, and worms, and therefore have the potential to achieve
therapeutic efficacy in infections by these microorganisms and/or
worms in the animals described herein. In an exemplary embodiment,
the bacteria is Gram-positive. In another exemplary embodiment, the
bacteria is a symbiont with another organism. In another exemplary
embodiment, the bacteria is a symbiont with a worm. In another
exemplary embodiment, the bacteria is a symbiont with an
arthropod.
IV. a) Inhibiting Microorganism Growth or Killing
Microorganisms
[0169] The compounds of the invention and/or combinations of the
invention exhibit potency against microorganisms, such as bacteria,
and therefore have the potential to treat, and/or prevent a
microorganism infection, or kill and/or inhibit the growth of
microorganisms.
[0170] In a further aspect, the invention provides a method of
inhibiting the growth of and/or killing a bacteria, the method
comprising contacting the bacteria with a compound of the
invention, or a pharmaceutically acceptable salt or a hydrate or a
solvate thereof, thereby inhibiting the growth of and/or killing
the bacteria. In an exemplary embodiment, the bacteria is
contacting with a therapeutically effective amount of the compound
of the invention. In an exemplary embodiment, the bacteria is
contacting with a prophylactically effective amount of the compound
of the invention.
[0171] In a further aspect, the invention provides a method of
treating and/or preventing a microorganism infection, or a method
of killing and/or inhibiting the growth of a microorganism, said
method comprising contacting said microorganism with an effective
amount of a compound of the invention, thereby killing and/or
inhibiting the growth of the microorganism. In a further aspect,
the invention provides a method of treating and/or preventing a
microorganism infection, or a method of killing and/or inhibiting
the growth of a microorganism, said method comprising contacting
said microorganism with an effective amount of a combination of the
invention, thereby killing and/or inhibiting the growth of the
microorganism.
[0172] In a further aspect, the invention provides a method of
treating and/or preventing a microorganism infection, or a method
of killing and/or inhibiting the growth of a microorganism, said
method comprising contacting said microorganism with a compound of
the invention, thereby killing and/or inhibiting the growth of the
microorganism. In a further aspect, the invention provides a method
of treating and/or preventing a microorganism infection, or a
method of killing and/or inhibiting the growth of a microorganism,
said method comprising contacting said microorganism with an
effective amount of a compound of the invention, thereby killing
and/or inhibiting the growth of the microorganism. In a further
aspect, the invention provides a method of treating and/or
preventing a microorganism infection, or a method of killing and/or
inhibiting the growth of a microorganism, said method comprising:
contacting said microorganism with an effective amount of a
combination of the invention, thereby killing and/or inhibiting the
growth of the microorganism.
[0173] In a further aspect, the invention provides a method of
treating a bacterial infection comprising administering to an
animal suffering from the infection an effective amount of a
compound of the invention or a combination of the invention, or a
pharmaceutically acceptable salt thereof, thereby treating the
bacterial infection. In an exemplary embodiment, the invention
provides a method of treating a bacterial infection comprising
administering to an animal suffering from the infection an
effective amount of a compound of the invention, or a
pharmaceutically acceptable salt thereof, and an effective amount
of an antibacterial, or a pharmaceutically acceptable salt thereof,
thereby treating the bacterial infection.
[0174] In a further aspect, the invention provides a method of
preventing a bacterial infection comprising administering to an
animal a prophylactic amount of a compound of the invention or a
combination of the invention, or a pharmaceutically acceptable salt
thereof, thereby treating the bacterial infection. In an exemplary
embodiment, the invention provides a method of preventing a
bacterial infection comprising administering to an animal a
prophylactic amount of a compound of the invention, or a
pharmaceutically acceptable salt thereof.
[0175] In an exemplary embodiment, the microorganism is a bacteria.
In an exemplary embodiment, the compound or combination is
described herein, or a salt, prodrug, hydrate or solvate thereof,
or a combination thereof. In an exemplary embodiment, the invention
provides a compound or combination described herein, or a salt,
hydrate or solvate thereof. In an exemplary embodiment, the
invention provides a compound or combination described herein, or a
prodrug thereof. In an exemplary embodiment, the invention provides
a compound or combination described herein, or a salt thereof. In
another exemplary embodiment, the compound or combination of the
invention is a compound or combination described herein, or a
pharmaceutically acceptable salt thereof. In another exemplary
embodiment, the compound or compound of the combination is
described by a formula listed herein, or a pharmaceutically
acceptable salt thereof. In an exemplary embodiment, the compound
is part of a combination described herein. In an exemplary
embodiment, the compound is part of a pharmaceutical formulation
described herein. In another exemplary embodiment, the contacting
occurs under conditions which permit entry of the compound into the
organism. Such conditions are known to one skilled in the art and
are described herein.
[0176] In another aspect, the microorganism is inside, and/or on
the surface of an animal. In an exemplary embodiment, the animal is
selected from the group consisting of human, cattle, deer,
reindeer, goat, honey bee, pig, sheep, horse, cow, bull, dog,
guinea pig, gerbil, rabbit, cat, camel, yak, elephant, ostrich,
otter, chicken, duck, goose, guinea fowl, pigeon, swan, and turkey.
In another exemplary embodiment, the animal is a human.
[0177] In an exemplary embodiment, the microorganism infection is
treated and or prevented, and/or the microorganism is killed or its
growth is inhibited, through oral administration of the compound of
the invention and/or the combination of the invention. In an
exemplary embodiment, the microorganism infection is treated and or
prevented, and/or the microorganism is killed or its growth is
inhibited through intravenous administration of the compound of the
invention and/or the combination of the invention.
[0178] In an exemplary embodiment, the microorganism is a bacteria.
In an exemplary embodiment, an infection is caused by and/or
associated with a microorganism, particularly a bacteria. In an
exemplary embodiment, the bacteria is a Gram-positive bacteria. In
another exemplary embodiment, the Gram-positive bacteria is
selected from the group consisting of Staphylococcus species,
Streptococcus species, Bacillus species, Mycobacterium species,
Corynebacterium species (Propionibacterium species), Clostridium
species, Actinomyces species, Enterococcus species, Streptomyces
species, Listeria species. In another exemplary embodiment, the
Gram-positive bacteria is selected from the group consisting of
Propionibacterium acnes, Staphylococcus aureus, Staphylococcus
epidermidis, Staphylococcus saprophyticus, Staphylococcus
haemolyticus, Streptococcus pyogenes, Streptococcus agalactiae,
Streptococcus pneumoniae, Enterococcus faecalis, Enterococcus
faecium, Bacillus anthracis, Mycobacterium avium-intracellulare,
Mycobacterium tuberculosis, Acinetobacter baumanii, Corynebacterium
diphtheria, Clostridium perfringens, Clostridium botulinum,
Clostridium tetani, Clostridium difficile, and Listeria
monocytogenes. In another exemplary embodiment, the Gram-positive
bacteria is selected from the group consisting of Staphylococcus
aureus, Staphylococcus epidermidis, Streptococcus pneumoniae,
Streptococcus pyogenes, Enterococcus faecalis, Enterococcus
faecium, Clostridium difficile and Propionibacter acnes. In an
exemplary embodiment, the bacteria is a coagulase positive
Staphylococci. In an exemplary embodiment, the bacteria is a
coagulase negative Staphylococci.
[0179] In an exemplary embodiment, the compounds of the invention
exhibit potency against bacteria which are associated with worms.
In an exemplary embodiment, the compounds of the invention exhibit
potency against bacteria which live inside of worms. In an
exemplary embodiment, the invention provides a method of killing
and/or inhibiting the growth of a bacteria which is associated with
a worm, comprising contacting the bacteria with an effective amount
of the compound of the invention, thereby killing and/or inhibiting
the growth of the bacteria. In an exemplary embodiment, the
bacteria is of the Wolbachia genus. In an exemplary embodiment, the
bacteria is Wolbachia pipientis.
IV. b) Inhibiting Worm Growth or Killing Worms
[0180] The compounds of the present invention exhibit potency
against certain worms as a consequence of their ability to kill the
endosymbiotic bacteria of the Wolbachia genus, and therefore have
the potential to kill and/or inhibit the growth of such worms. The
invention therefore provides a method of killing a worm, comprising
contacting the worm with an effective amount of the compound of the
invention, thereby killing the worm. The invention provides a
method of inhibiting the growth of a worm, comprising contacting
the worm with an effective amount of the compound of the invention,
thereby inhibiting the growth of the worm. In an exemplary
embodiment, the worm is female. In an exemplary embodiment, the
worm is male. In an exemplary embodiment, the worm is a
hermaphrotide. In an exemplary embodiment, the worm is an egg. In
an exemplary embodiment, the worm is an unfertilized egg. In an
exemplary embodiment, the worm is fertilized egg. In an exemplary
embodiment, the worm is a larvae. In an exemplary embodiment, the
worm is mature. In an exemplary embodiment, the worm is fully
mature. In an exemplary embodiment, the worm is contacted with the
compound of the invention inside an animal. In an exemplary
embodiment, the worm is contacted with the compound of the
invention outside of an animal.
[0181] In an exemplary embodiment, the worm is a parasitic worm. In
an exemplary embodiment, the worm is a helminth. In an exemplary
embodiment, the worm is a nematode. In an exemplary embodiment, the
nematode is a filarid. In an exemplary embodiment, the nematode is
a member of Filarioidea. In an exemplary embodiment, the nematode
is a member of Onchocercinae. In an exemplary embodiment, the
nematode is a member of Dirofilariinae. In an exemplary embodiment,
the nematode is a filarid. In an exemplary embodiment, the nematode
is a filarial worm. In an exemplary embodiment, the nematode is a
member of the genus Wuchereria. In an exemplary embodiment, the
nematode is Wuchereria bancrofti. In an exemplary embodiment, the
nematode is a member of the genus Brugia. In an exemplary
embodiment, the nematode is Brugia malayi. In an exemplary
embodiment, the nematode is Brugia timori. In an exemplary
embodiment, the Brugia is a microfilariae. In an exemplary
embodiment, the Brugia is a larvae. In an exemplary embodiment, the
Brugia is mature. In an exemplary embodiment, the Brugia is
contacted by the compound of the invention in the skin of the
animal. In an exemplary embodiment, the Brugia is contacted by the
compound of the invention in the lymphatic system of the animal. In
an exemplary embodiment, the Brugia is contacted by the compound of
the invention in the blood of the animal. In an exemplary
embodiment, the Brugia is contacted by the compound of the
invention in the muscle of the animal. In an exemplary embodiment,
the Brugia is contacted by the compound of the invention in the
salivary gland of the animal.
[0182] In an exemplary embodiment, the nematode is a member of the
genus Mansonella. In an exemplary embodiment, the nematode is
selected from the group consisting of Mansonella streptocerca,
Mansonella perstans, and Mansonella ozzardi. In an exemplary
embodiment, the nematode is a member of the genus Onchocerca. In an
exemplary embodiment, the nematode is Onchocerca volvulus. In an
exemplary embodiment, the nematode is Onchocerca ochengi.
[0183] In an exemplary embodiment, the nematode is a heartworm. In
an exemplary embodiment, the nematode is a member of the genus
Dirofilaria. In an exemplary embodiment, the nematode is
Dirofilaria immitis. In an exemplary embodiment, the nematode is
Dirofilaria tenuis or Dirofilaria repens.
IV. c) Diseases
[0184] The compounds of the invention and/or combinations of the
invention exhibit potency against microorganisms, such as bacteria,
and therefore have the potential to achieve therapeutic efficacy in
the animals described herein. The compounds of the invention and/or
combinations of the invention exhibit potency against worms, and
therefore have the potential to achieve therapeutic efficacy in the
animals described herein.
[0185] In another aspect, the invention provides a method of
treating and/or preventing a disease. In an exemplary embodiment,
the method includes administering to the animal a therapeutically
and/or prophylactically effective amount of a compound of the
invention, sufficient to treat and/or prevent the disease. In an
exemplary embodiment, the method includes administering to the
animal a therapeutically and/or prophylactically effective amount
of a combination of the invention, sufficient to treat and/or
prevent the disease. In an exemplary embodiment, the animal being
administered the compound is not otherwise in need of treatment
with a compound of the invention.
[0186] In an exemplary embodiment, the compound of the invention or
the combination of the invention can be used in human or veterinary
medical therapy, particularly in the treatment or prophylaxis of
bacterial-associated disease. In an exemplary embodiment, the
compound of the invention or the combination of the invention can
be used in human or veterinary medical therapy, particularly in the
treatment of a Gram-positive bacterial-associated disease. In an
exemplary embodiment, the compound of the invention or the
combination of the invention can be used in human or veterinary
medical therapy, particularly in the prophylaxis of a Gram-positive
bacterial-associated disease. In an exemplary embodiment, the
compound of the invention or the combination of the invention can
be used in human or veterinary medical therapy, particularly in the
treatment of a Wolbachia-associated disease. In an exemplary
embodiment, the compound of the invention or the combination of the
invention can be used in human or veterinary medical therapy,
particularly in the prophylaxis of a Wolbachia-associated disease.
In another exemplary embodiment, the disease is pneumonia. In
another exemplary embodiment, the disease is hospital-acquired
pneumonia. In another exemplary embodiment, the disease is
hospital-associated pneumonia. In another exemplary embodiment, the
disease is community-acquired pneumonia. In another exemplary
embodiment, the disease is a acute bacterial skin and
skin-structure infection (ABSSSI). In another exemplary embodiment,
the disease is bacteremia. In another exemplary embodiment, the
disease is endocarditis. In another exemplary embodiment, the
disease is osteomyelitis. In an exemplary embodiment, the disease
is associated with a Staphylococcus species. In another exemplary
embodiment, the disease is selected from the group consisting of
pneumonia, gastroenteritis, toxic shock syndrome, community
acquired pneumonia (CAP), meningitis, septic arthritis, urinary
tract infection, bacteremia, endocarditis, osteomylitis, skin and
skin-structure infection. In an exemplary embodiment, the disease
is associated with a Streptococcus species. In another exemplary
embodiment, the disease is selected from the group consisting of
strep throat, skin infections, necrotizing fasciitis, toxic shock
syndrome, pneumonia, otitis media and sinusitis. In an exemplary
embodiment, the disease is associated with an Actinomyces species.
In another exemplary embodiment, the disease is actinomycosis. In
an exemplary embodiment, the disease is associated with a Norcardia
species. In another exemplary embodiment, the disease is pneumonia.
In an exemplary embodiment, the disease is associated with a
Corynebacterium species. In another exemplary embodiment, the
disease is diptheria. In an exemplary embodiment, the disease is
associated with a Listeria species. In another exemplary
embodiment, the disease is meningitis. In an exemplary embodiment,
the disease is associated with a Bacillus species. In another
exemplary embodiment, the disease is anthrax or food poisoning. In
an exemplary embodiment, the disease is associated with a
Clostridium species. In another exemplary embodiment, the disease
is selected from the group consisting of botulism, tetanus, gas
gangrene and diarrhea. In an exemplary embodiment, the disease is
associated with a Mycobacterium species. In another exemplary
embodiment, the disease is tuberculosis or leprosy. In an exemplary
embodiment, the disease is associated with a Listeria species. In
an exemplary embodiment, the disease is associated with a Wolbachia
species. In an exemplary embodiment, the disease is associated with
Wolbachia pipientis. In an exemplary embodiment, the disease is
selected from the group consisting of candidiasis, aspergillosis,
coccidioidomycosis, cryptococcosis, histoplasmosis, blastomycosis,
paracoccidioidomycosis, zygomycosis, phaeohyphomycosis and
rhinosporidiosis.
[0187] In an exemplary embodiment, the compound of the invention
can be used in human medical therapy, particularly in the treatment
of worm-associated disease. In an exemplary embodiment, the
compound of the invention can be used in human medical therapy,
particularly in the prophylaxis of worm-associated disease. In an
exemplary embodiment, the compound of the invention can be used in
veterinary medical therapy, particularly in the treatment of
worm-associated disease. In an exemplary embodiment, the compound
of the invention can be used in veterinary medical therapy,
particularly in the prophylaxis of worm-associated disease. In an
exemplary embodiment, the compound of the invention can be used in
human medical therapy, particularly in the treatment of
helminth-associated disease. In an exemplary embodiment, the
compound of the invention can be used in human medical therapy,
particularly in the prophylaxis of helminth-associated disease. In
an exemplary embodiment, the compound of the invention can be used
in veterinary medical therapy, particularly in the treatment of
helminth-associated disease. In an exemplary embodiment, the
compound of the invention can be used in veterinary medical
therapy, particularly in the prophylaxis of helminth-associated
disease. In an exemplary embodiment, the disease is associated with
a worm. In an exemplary embodiment, the disease is caused by a
worm. In an exemplary embodiment, the disease is associated with a
worm described herein. In an exemplary embodiment, the disease is
associated with a nematode. In an exemplary embodiment, the disease
is associated with a nematode described herein. In an exemplary
embodiment, the nematode is Wuchereria bancrofti. In an exemplary
embodiment, the nematode is Brugia malayi. In an exemplary
embodiment, the nematode is Brugia timori. In an exemplary
embodiment, the nematode is Dirofilaria immitis. In an exemplary
embodiment, the disease is a member selected from enterobiasis,
filariasis, and onchocerciasis. In an exemplary embodiment, the
disease is lymphatic filariasis. In an exemplary embodiment, the
disease is bancroftian filariasis. In an exemplary embodiment, the
disease is lymphadenitis. In an exemplary embodiment, the disease
is lymphangitis. In an exemplary embodiment, the disease is
lymphedema. In an exemplary embodiment, the disease is subcutaneous
filariasis. In an exemplary embodiment, the disease is serious
cavity filariasis. In an exemplary embodiment, the disease is
elephantiasis. In an exemplary embodiment, the disease is
elephantiasis tropica. In an exemplary embodiment, the disease is
onchocerciasis.
[0188] In another exemplary embodiment, the animal is selected from
the group consisting of human, cattle, deer, reindeer, goat, honey
bee, pig, sheep, horse, cow, bull, dog, guinea pig, gerbil, rabbit,
cat, camel, yak, elephant, ostrich, otter, chicken, duck, goose,
guinea fowl, pigeon, swan, and turkey. In another exemplary
embodiment, the animal is a human. In another exemplary embodiment,
the animal is selected from the group consisting of a human,
cattle, goat, pig, sheep, horse, cow, bull, dog, guinea pig,
gerbil, rabbit, cat, chicken and turkey. In another exemplary
embodiment, the disease is a systemic disease. In another exemplary
embodiment, the disease is a topical disease.
[0189] In an exemplary embodiment, the disease is treated through
oral administration of a compound of the invention and/or a
combination of the invention. In an exemplary embodiment, the
disease is treated through intravenous administration of a compound
of the invention and/or a combination of the invention. In an
exemplary embodiment, the disease is treated through intramuscular
administration of a compound of the invention and/or a combination
of the invention. In an exemplary embodiment, the disease is
treated through topical administration of a compound of the
invention and/or a combination of the invention.
[0190] In an exemplary embodiment, for any of the methods described
herein, a compound of the invention, a combination of the
invention, a compound described herein or a pharmaceutically
acceptable salt thereof, or combination described herein, and/or a
pharmaceutical formulation described herein can be used.
V. Pharmaceutical Formulations
[0191] In another aspect, the invention is a pharmaceutical
formulation which includes: (a) a pharmaceutically acceptable
excipient; and (b) a compound of the invention. In another aspect,
the pharmaceutical formulation includes: (a) a pharmaceutically
acceptable excipient; and (b) a compound according to a formula
described herein. In another aspect, the pharmaceutical formulation
includes: (a) a pharmaceutically acceptable excipient; and (b) a
compound described herein, or a salt, prodrug, hydrate or solvate
thereof. In another aspect, the pharmaceutical formulation
includes: (a) a pharmaceutically acceptable excipient; and (b) a
compound described herein, or a salt, hydrate or solvate thereof.
In another aspect, the pharmaceutical formulation includes: (a) a
pharmaceutically acceptable excipient; and (b) a compound described
herein, or a salt, hydrate or solvate thereof. In another aspect,
the pharmaceutical formulation includes: (a) a pharmaceutically
acceptable excipient; and (b) a salt of a compound described
herein. In an exemplary embodiment, the salt is a pharmaceutically
acceptable salt. In another aspect, the pharmaceutical formulation
includes: (a) a pharmaceutically acceptable excipient; and (b) a
prodrug of a compound described herein. In another aspect, the
pharmaceutical formulation includes: (a) a pharmaceutically
acceptable excipient; and (b) a compound described herein. In an
exemplary embodiment, the pharmaceutical formulation is a unit
dosage form. In an exemplary embodiment, the pharmaceutical
formulation is a single unit dosage form.
[0192] Information regarding excipients of use in the formulations
of the invention can be found in Remington: The Science and
Practice of Pharmacy, 21st Ed., Pharmaceutical Press (2011) which
is incorporated herein by reference.
[0193] Exemplary embodiments are summarized herein below.
[0194] In an exemplary embodiment, the invention provides a
compound, or a salt or a hydrate or a solvate thereof, having a
structure according to the following formula:
##STR00106##
wherein W is H or a bond to X; X is
##STR00107##
wherein R.sup.a and R.sup.b are each independently selected from
the group consisting of R.sup.15, --OR.sup.15, --NR.sup.15R.sup.16,
--SR.sup.15, --S(O)R.sup.15, --S(O).sub.2R.sup.15,
--S(O).sub.2NR.sup.15R.sup.16, --C(O)R.sup.15, --C(O)OR.sup.15, and
--C(O)NR.sup.15R.sup.16 wherein R.sup.15 and R.sup.16 are each
independently selected from the group consisting of H, halogen,
cyano, nitro, --OR.sup.17, --NR.sup.17R.sup.18, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl, wherein R.sup.17 and
R.sup.18 are each independently selected from the group consisting
of H, substituted or unsubstituted alkyl, substituted or
unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl,
substituted or unsubstituted heterocycloalkyl, substituted or
unsubstituted aryl, and substituted or unsubstituted heteroaryl,
and wherein R.sup.15 and R.sup.16, and/or R.sup.17 and R.sup.18,
along with the nitrogen to which they are connected, are optionally
joined to form a substituted or unsubstituted 4- to 8-membered
ring, with the proviso that R.sup.a and R.sup.b are not both H; or
X is
##STR00108##
wherein R.sup.c is --OR.sup.15, --NR.sup.15R.sup.16, --SR.sup.15,
--S(O)R.sup.15, --S(O).sub.2R.sup.15, --S(O).sub.2N.sup.15R.sup.16,
--C(O)R.sup.15, --C(O)OR.sup.15, and --C(O)NR.sup.15R.sup.16
wherein R.sup.15 and R.sup.16 are each independently selected from
the group consisting of H, halogen, cyano, nitro, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl, and wherein R.sup.15
and R.sup.16, along with the nitrogen to which they are connected,
are optionally joined to form a substituted or unsubstituted 4- to
8-membered ring; or X is
##STR00109##
wherein R.sup.d and R.sup.e are each independently selected from
the group consisting of H, halogen, cyano, nitro, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl, --OR.sup.15,
--NR.sup.15R.sup.16, --SR.sup.15, --S(O)R.sup.15,
--S(O).sub.2R.sup.15, --S(O).sub.2N.sup.15R.sup.16, --C(O)R.sup.15,
--C(O)OR.sup.15, and --C(O)N.sup.15R.sup.16, wherein R.sup.15 and
R.sup.16 are each independently selected from the group consisting
of H, halogen, cyano, nitro, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, and
substituted or unsubstituted heteroaryl and wherein R.sup.d and
R.sup.e, along with the atom to which they are connected, are
optionally joined to form a substituted or unsubstituted 3- to
8-membered ring and wherein R.sup.15 and R.sup.16, along with the
nitrogen to which they are connected, are optionally joined to form
a substituted or unsubstituted 4- to 8-membered ring with the
proviso that R.sup.d and R.sup.e are not both H, wherein X
optionally comprises an attachment point to W; Y is selected from
the group consisting of a bond, --O--, --S--, --NH--, substituted
or unsubstituted alkylene, and substituted or unsubstituted
heteroalkylene; and Z is a substituted or unsubstituted
heterocyclic ring or ring system containing at least one endocyclic
boron.
[0195] In an exemplary embodiment, according to the above
paragraph, the compound, or a salt or a hydrate or a solvate
thereof, wherein said X is
##STR00110##
wherein R.sup.15 is selected from the group consisting of H,
substituted or unsubstituted alkyl, substituted or unsubstituted
heteroalkyl, substituted or unsubstituted cycloalkyl, substituted
or unsubstituted heterocycloalkyl, substituted or unsubstituted
aryl, and substituted or unsubstituted heteroaryl.
[0196] In an exemplary embodiment, according to any of the above
paragraphs, for the compound, or a salt or a hydrate or a solvate
thereof, wherein said X is
##STR00111##
wherein R.sup.15 and R.sup.16 are each independently selected from
the group consisting of H, --OR.sup.17, --NR.sup.17R.sup.18,
substituted or unsubstituted alkyl, substituted or unsubstituted
heteroalkyl, substituted or unsubstituted cycloalkyl, substituted
or unsubstituted heterocycloalkyl, substituted or unsubstituted
aryl, and substituted or unsubstituted heteroaryl, wherein R.sup.17
and R.sup.18 are each independently selected from the group
consisting of H, substituted or unsubstituted alkyl, substituted or
unsubstituted heteroalkyl, substituted or unsubstituted cycloalkyl,
substituted or unsubstituted heterocycloalkyl, substituted or
unsubstituted aryl, and substituted or unsubstituted heteroaryl,
and wherein R.sup.15 and R.sup.16, and/or R.sup.17 and R.sup.18,
along with the nitrogen to which they are connected, are optionally
joined to form a substituted or unsubstituted 4- to 8-membered
ring.
[0197] In an exemplary embodiment, according to any of the above
paragraphs, for the compound, or a salt or a hydrate or a solvate
thereof, wherein said X is
##STR00112##
wherein R.sup.c is selected from the group consisting of H,
substituted or unsubstituted alkyl, and --OR.sup.15 wherein
R.sup.15 is H or substituted or unsubstituted alkyl.
[0198] In an exemplary embodiment, according to any of the above
paragraphs, for the compound, or a salt or a hydrate or a solvate
thereof, wherein said X is
##STR00113##
wherein R.sup.d is selected from the group consisting of halogen,
substituted or unsubstituted alkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, --OR.sup.15,
--SR.sup.15, --S(O)R.sup.1, --NR.sup.15R.sup.16, --C(O)R.sup.15,
--CH.sub.2C(O)OR.sup.15, and --CH.sub.2C(O)NR.sup.15R.sup.16
wherein R.sup.15 and R.sup.16 are each independently selected from
the group consisting of H, substituted or unsubstituted alkyl,
substituted or unsubstituted heteroalkyl, substituted or
unsubstituted cycloalkyl, substituted or unsubstituted
heterocycloalkyl, substituted or unsubstituted aryl, and
substituted or unsubstituted heteroaryl and wherein R.sup.15 and
R.sup.16, along with the nitrogen to which they are connected, are
optionally joined to form a substituted or unsubstituted 4- to
8-membered ring.
[0199] In an exemplary embodiment, according to any of the above
paragraphs, the compound, or a salt or a hydrate or a solvate
thereof, wherein R.sup.d comprises said attachment point to W.
[0200] In an exemplary embodiment, according to any of the above
paragraphs, the compound, or a salt or a hydrate or a solvate
thereof, wherein said Y is *--OCH.sub.2- or *--SCH.sub.2-- or
*--NHCH.sub.2-- or *--CH.sub.2NH-- or *--C(O)NH--, wherein *
represents the attachment point to said Z.
[0201] In an exemplary embodiment, according to any of the above
paragraphs, the compound, or a salt or a hydrate or a solvate
thereof, wherein said Z is selected from the group consisting of
substituted or unsubstituted benzoxaborole, substituted or
unsubstituted pyridinyloxaborole, substituted or unsubstituted
benzoxaborininol, substituted or unsubstituted benzoxazaborininol,
substituted or unsubstituted benzodiazaborininol, and substituted
or unsubstituted oxaborole.
[0202] In an exemplary embodiment, according to any of the above
paragraphs, the compound, or a salt or a hydrate or a solvate
thereof, wherein said Z is
##STR00114##
wherein R.sup.3, R.sup.3a, R.sup.4, R.sup.5, and R.sup.7 are each
independently selected from the group consisting of R.sup.1,
--OR.sup.10, --NR.sup.10R.sup.11, --SR.sup.10, --S(O)R.sup.10,
--S(O).sub.2R.sup.10, --S(O).sub.2NR.sup.10R.sup.11,
--C(O)R.sup.10, --C(O)OR.sup.10, and --C(O)NR.sup.10R.sup.11
wherein R.sup.10 and R.sup.11 are each independently selected from
the group consisting of H, halogen, cyano, nitro, substituted or
unsubstituted alkyl, substituted or unsubstituted heteroalkyl,
substituted or unsubstituted cycloalkyl, substituted or
unsubstituted heterocycloalkyl, substituted or unsubstituted aryl,
and substituted or unsubstituted heteroaryl.
[0203] In an exemplary embodiment, according to any of the above
paragraphs, the compound, or a salt or a hydrate or a solvate
thereof, wherein said Z is
##STR00115##
wherein R.sup.4, R.sup.5, and R.sup.7 are each independently
selected from the group consisting of R.sup.10, --OR.sup.10,
--NR.sup.10R.sup.11, wherein R.sup.10 and R.sup.11 are each
independently selected from the group consisting of H, halogen,
cyano, nitro, substituted or unsubstituted alkyl, and substituted
or unsubstituted heteroalkyl.
[0204] In an exemplary embodiment, according to any of the above
paragraphs, the compound, or a salt or a hydrate or a solvate
thereof, compound of claim 10, or a salt or a hydrate or a solvate
thereof, wherein said Z is
##STR00116##
[0205] In an exemplary embodiment, according to any of the above
paragraphs, the compound, or a salt or a hydrate or a solvate
thereof, which is
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-7-(hydroxymethyl)-4,7,9,1-
2-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fl-
uoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate.
[0206] In an exemplary embodiment, according to any of the above
paragraphs, the compound, or a salt or a hydrate or a solvate
thereof, which is
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-((-
R)-oxiran-2-yl)-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7--
fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate.
[0207] In an exemplary embodiment, according to any of the above
paragraphs, the compound, or a salt or a hydrate or a solvate
thereof, which is
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-((-
E)-2-(3-methyl-1,2,4-oxadiazol-5-yl)vinyl)-3-oxodecahydro-4,9a-propanocycl-
openta[8]annulen-5-yl
2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate.
[0208] In an exemplary embodiment, the invention provides a
combination comprising: the compound of a preceding claim, or a
pharmaceutically acceptable salt thereof, together with at least
one other therapeutically active agent.
[0209] In an exemplary embodiment, according to the above
combination paragraph, wherein the other therapeutically active
agent is an anti-bacterial agent.
[0210] In an exemplary embodiment, the invention provides a
pharmaceutical formulation comprising: a) the compound of a
preceding claim, or a pharmaceutically acceptable salt or a hydrate
or a solvate thereof, and b) a pharmaceutically acceptable
excipient.
[0211] In an exemplary embodiment, according to the above
pharmaceutical formulation paragraph, the pharmaceutical
formulation is an oral formulation or an intravenous
formulation.
[0212] In an exemplary embodiment, according to any of the above
paragraphs, the salt of the compound according to any of the above
paragraphs is a pharmaceutically acceptable salt.
[0213] In an exemplary embodiment, the invention is a method of
inhibiting protein synthesis in a bacteria, the method comprising
contacting the bacteria with the compound in any of the above
paragraphs, or a pharmaceutically acceptable salt or a hydrate or a
solvate thereof, thereby inhibiting protein synthesis in the
bacteria.
[0214] In an exemplary embodiment, the invention is a method of
inhibiting the growth of and/or killing a bacteria, the method
comprising contacting the bacteria with the compound in any of the
above paragraphs, or a pharmaceutically acceptable salt or a
hydrate or a solvate thereof, thereby inhibiting the growth of
and/or killing the bacteria.
[0215] In an exemplary embodiment, according to any of the above
method paragraphs, wherein the bacteria is Gram-positive.
[0216] In an exemplary embodiment, according to any of the above
method paragraphs, wherein the bacteria is Staphylococcus aureus or
Streptococcus pneumoniae.
[0217] In an exemplary embodiment, according to any of the above
method paragraphs, wherein the bacteria is methicillin-resistant
Staphylococcus aureus.
[0218] In an exemplary embodiment, according to any of the above
method paragraphs, wherein the bacteria is of the Wolbachia
genus.
[0219] In an exemplary embodiment, according to any of the above
method paragraphs, wherein the bacteria is Wolbachia pipientis.
[0220] In an exemplary embodiment, the invention is a method of
treating a disease in an animal in need of the treatment, the
method comprising administering to the animal a therapeutically
effective amount of the compound in any of the above paragraphs, or
a pharmaceutically acceptable salt or a hydrate or a solvate
thereof, thereby treating the disease.
[0221] In an exemplary embodiment, according to the above method
paragraph, wherein the disease is associated with a Gram-positive
bacteria.
[0222] In an exemplary embodiment, according to any of the above
method paragraphs, wherein the disease is pneumonia.
[0223] In an exemplary embodiment, according to any of the above
method paragraphs, wherein the disease is onchocerciasis.
[0224] In an exemplary embodiment, according to any of the above
method paragraphs, the animal is a human.
[0225] In an exemplary embodiment, according to any of the above
method paragraphs, there is a proviso that the animal is not
otherwise in need of treatment with a compound of the
invention.
[0226] The invention is further illustrated by the Examples that
follow. The Examples are not intended to define or limit the scope
of the invention.
EXAMPLES
[0227] Proton NMR are recorded on Varian AS 300 spectrometer and
chemical shifts are reported as .delta. (ppm) down field from
tetramethylsilane. Mass spectra are determined on Micromass Quattro
II.
Example 1
[0228] 1.
(4aR,6R,7R,7aR,10aS,11R,11aS,14R)-4a,7,11,14-tetramethyl-2,8-dioxododecah-
ydro-2H-7,10a-propanocyclopenta[6,7]cycloocta[1,2-b]pyran-6-yl2-((7-fluoro-
-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate [0229]
2.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-(3-amino-3-oxopropyl)-8-hydroxy-4,7,9,12-t-
etramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluor-
o-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
[0230] 3.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-(3-(methyla-
mino)-3-oxopropyl)-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(-
(7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
[0231] 4.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-(3-(ethylamino)-3-oxopropyl)-8-h-
ydroxy-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annule-
n-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)ace-
tate [0232] 5.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-(3-(butylamino)-3-oxopropyl)-8-hydroxy-4,7-
,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((-
7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
[0233] 6.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-(3-(cyclopropylamino)-3-oxopropy-
l)-8-hydroxy-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]-
annulen-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)o-
xy)acetate [0234] 7.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-7-(3-(3-hydroxypyrrolidin-1-yl)-3--
oxopropyl)-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]an-
nulen-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy-
)acetate [0235] 8.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-7-(3-((S)-3-hydroxypyrrolidin-1-yl-
)-3-oxopropyl)-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[-
8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl-
)oxy)acetate
##STR00117## ##STR00118##
[0236] TosCl (55.5 g, 291.3 mmol, 1.1 eq) was added to a solution
of
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-7-vinyl-
decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-hydroxyacetate
(104.0 g, 274.8 mmol, 1.0 eq), TEA (36.2 g, 357.2 mmol, 1.3 eq) and
Py. (3.0 g, 38.5 mmol, 0.1 eq) in DCM (500 mL) at 0.degree. C. The
mixture was stirred at 15.degree. C. for 3 hours. The mixture was
filtered, the filtrate was treated with 2N aq. HCl till pH<4.
The aqueous layer was treated with DCM (50 mL.times.3). The
combined organic phase was treated with brine 100 mL.times.1, dried
over Na.sub.2SO.sub.4 and concentrated in vacuo. The crude product
was dissolved in DCM 300 mL, petroleum ether (100 mL) was added to
the mixture. Yellow solid was precipitated and filtered to give
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-7-vinyl-
decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)acetate
(93.0 g, 174.6 mmol, 63.5% yield) as yellow solid. .sup.1H NMR
(DMSO-d.sub.6, 400 MHz) .delta. 7.80 (d, J=8.2 Hz, 2H), 7.47 (d,
J=8.0 Hz, 2H), 6.05 (dd, J=17.8, 11.2 Hz, 1H), 5.53 (d, J=8.4 Hz,
1H), 4.96-5.09 (m, 2H), 4.59-4.81 (m, 2H), 3.40 (d, J=5.6 Hz, 1H),
2.41 (s, 2H), 2.39 (s, 1H), 1.95-2.24 (m, 6H), 1.41-1.75 (m, 4H),
1.30 (s, 3H), 1.18-1.27 (m, 3H), 1.03 (s, 3H), 0.92-0.99 (m, 1H),
0.81 (d, J=7.0 Hz, 3H), 0.50 (d, J=7.0 Hz, 3H).
[0237]
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-7-
-vinyldecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)acetate
(30.0 g, 56.3 mmol, 1.0 eq) in DCM (2.0 L) was bubbled into ozone
(2.7 g, 56.3 mmol, 1.0 eq) at -78.degree. C. for 2 hours. The
mixture was bubbled with nitrogen for 10 mins and quenched by the
addition of TEA (57.0 g, 563.2 mmol, 10.0 eq) at -78.degree. C.,
the blue solution turned to colorless. The mixture was warmed to
room temperature; wet starch potassium iodide paper didn't change.
The solvent was concentrated, 2N HCl aq. solution was added to the
mixture until pH<4. The aqueous solution was treated with DCM
(100 mL.times.3). The combined organic was washed with brine 200
mL.times.1, dried over Na.sub.2SO.sub.4 and concentrated in vacuo
to give
3aR,4R,5R,7R,8S,9R,9aS,12R)-7-formyl-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-
decahydro-4,9a-propanocyclopenta [8]annulen-5-yl2-(tosyloxy)acetate
(29.0 g, 54.2 mmol, 96.3% yield) as white foam.
[0238] LiHMDS (1 M, 14.96 mL, 1.00 eq) was added to a solution of
methyl 2-diethoxyphosphorylacetate (3.46 g, 16.46 mmol, 1.10 eq) in
THE (100.00 mL) at -78.degree. C., the mixture was stirred at this
temperature for 1 hour, then
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-formyl-8-hydroxy-4,7,9,12-tetramethyl-3-ox-
odecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)acetate
(8.0 g, 15.0 mmol, 1.0 eq) in 5 mL THE was added to the mixture
dropwise at -78.degree. C. Then the mixture warmed to 15.degree.
C., and stirred at 15.degree. C. for 3 hours. 100 mL water was
added to the mixture, the aqueous phase was treated with EtOAc (50
mL.times.3). The combined organic phase was washed with brine 50
mL.times.1, dried over Na.sub.2SO.sub.4 and concentrated in vacuo
to give crude product, which was purified by flash column
chromatography (petroleum ether/EtOAc=3:1) to give (E)-methyl
3-((3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-5-(2-
-(tosyloxy)acetoxy)decahydro-4,9a-propanocyclopenta[8]annulen-7-yl)acrylat-
e (6.4 g, 10.8 mmol, 72.4% yield) as white foam.
[0239]
(E)-methyl3-((3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetram-
ethyl-3-oxo-5-(2-(tosyloxy)acetoxy)decahydro-4,9a-propanocyclopenta[8]annu-
len-7-yl)acrylate (6.4 g, 10.8 mmol, 1.0 eq) and Pd/C (2.0 g) in
MeOH (200.0 mL) were stirred at 50.degree. C. for 60 hours under 50
Psi hydrogen atmosphere. The mixture was filtered and the filtrate
was concentrated in vacuo to give crude
(4aR,6R,7R,7aR,10aS,11R,11aS,14R)-4a,7,11,14-tetramethyl-2,8-dioxododecah-
ydro-2H-7,10a-propanocyclopenta[6,7]cycloocta[1,2-b]pyran-6-yl2-(tosyloxy)-
acetate (5.5 g, 9.8 mmol, 90.6% yield) as white foam.
[0240]
(4aR,6R,7R,7aR,10aS,11R,11aS,14R)-4a,7,11,14-tetramethyl-2,8-dioxod-
odecahydro-2H-7,10a-propanocyclopenta[6,7]cycloocta[1,2-b]pyran-6-yl2-(tos-
yloxy)acetate (2.2 g, 3.9 mmol, 1.0 eq), 7-fluoro-1-hydroxy-3H-2,
1-benzoxaborol-6-ol (658.9 mg, 3.9 mmol, 1.0 eq) and
Na.sub.2CO.sub.3 (1.3 g, 11.8 mmol, 3.0 eq) in DMSO (30.0 mL) were
heated to 30-40.degree. C. for 12 hours. Water (20 mL) was added to
the mixture, white solid was precipitated. The mixture was filtered
to give crude product (.about.2.5 g crude). .about.500 mg crude
product was purified by prep-HPLC (column: Luna C18 100.times.30
mm, 5 .mu.m; liquid phase: [A-TFA/H.sub.2O=0.075% v/v; B-ACN]B %:
35%-50%, 18 min]). The solvent was concentrated to about 15 mL, and
dried by lyophilizer to give
(4aR,6R,7R,7aR,10aS,11R,11aS,14R)-4a,7,11,14-tetramethyl-2,8-dioxododecah-
ydro-2H-7,10a-propanocyclopenta[6,7]cycloocta[1,2-b]pyran-6-yl2-((7-fluoro-
-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (53
mg) as white solid. .sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta.
9.27 (s, 1H), 7.24 (t, J=8.0 Hz, 1H), 7.11 (d, J=8.0 Hz, 1H), 5.54
(d, J=7.6 Hz, 1H), 4.92 (s, 2H), 4.83 (s, 2H), 4.39 (d, J=5.6 Hz,
1H), 2.42 (s, 1H), 2.35-2.00 (m, 4H), 1.86-1.23 (m, 12H), 1.21-0.95
(m, 6H), 0.88 (d, J=6.6 Hz, 3H), 0.65 (d, J=7.1 Hz, 3H). MS (ESI):
mass calcd. for C.sub.30H.sub.38BFO.sub.8 556.4, m/z found 573.3
[M+18-H]. HPLC: 100% in 220 nm; 100% in 254 nm.
[0241]
(4aR,6R,7R,7aR,10aS,11R,11aS,14R)-4a,7,11,14-tetramethyl-2,8-dioxod-
odecahydro-2H-7,10a-propanocyclopenta[6,7]cycloocta[1,2-b]pyran-6-yl2-((7--
fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(300.0 mg, 539.2 umol, 1.0 eq) in amine (15.0 eq) and MeOH (10 mL)
were stirred at 50.degree. C. for 12 hours. The mixture was
concentrated in vacuo to give crude product, which was purified by
prep-HPLC (Instrument: Gilson 281 semi-preparative HPLC system
Mobile phase: A: 6.6 mM NH.sub.4HCO.sub.3 in H.sub.2O; B: ACN
Column: Durashell C18 150.times.25 mm, 5 .mu.m, 100 A Flow rate: 20
ml/min; Monitor wavelength: 220&254 nm Gradient: 10-100 B %,
time: 0-18.4) to give product
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-(3-amino-3-oxopropyl)-8-hydroxy-4,7,9,12-t-
etramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluor-
o-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (66.0
mg, 109.1 umol, 20.2% yield, 94.7% purity) as white solid. .sup.1H
NMR (DMSO-d.sub.6, 400 MHz) .delta. 9.25 (br. s., 1H), 7.26-7.16
(m, 2H), 7.14-7.08 (m, 1H), 6.68 (br. s., 1H), 5.55 (d, J=7.9 Hz,
1H), 4.92 (s, 1H), 4.85-4.75 (m, 2H), 4.46 (d, J=6.2 Hz, 1H), 3.37
(br. s., 1H), 2.30-1.97 (m, 4H), 1.78-1.11 (m, 12H), 1.09-0.74 (m,
11H), 0.64 (d, J=7.1 Hz, 3H). MS (ESI): mass calcd. for
C.sub.30H.sub.41BFNO.sub.8 573.3, m/z found 572.3 [M-H].sup.-.
HPLC: 94.7% in 220 nm; 54.2% in 254 nm.
[0242]
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-(3-(m-
ethylamino)-3-oxopropyl)-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-
-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetat-
e: Prep-HPLC condition: The residue was purified by prep-HPLC
(column: Luna C8 100.times.30 mm, 5 .mu.m; liquid phase:
[A-TFA/H.sub.2O=0.075% v/v; B-ACN]B %: 30%-60%, 12 min]). The
solvent was concentrated to about 20 mL solution left and dried
over lyophilize to give
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-(3-(methyla-
mino)-3-oxopropyl)-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(-
(7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(73.0 mg, 120.1 umol, 22.3% yield, 96.7% purity) as white solid.
.sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 7.71 (br. s., 1H),
7.21-7.15 (m, 2H), 7.12-7.00 (m, 1H), 5.55 (br. s., 1H), 4.92 (s,
1H), 4.80-4.40 (m, 2H), 4.40 (s, 1H), 3.35 (d, J=4.4 Hz, 1H),
2.55-3.21 (m, 3H), 2.19-2.05 (m, 7H), 1.68-1.28 (m, 12H), 0.85-0.80
(m, 8H), 0.65-0.63 (m, 3H). MS (ESI): mass calcd. for
C.sub.31H.sub.43BFNO.sub.8 587.3, m/z found 586.3 [M-H].sup.-.
HPLC: 96.7% in 220 nm; 100% in 254 nm.
[0243]
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-(3-(ethylamino)-3-oxopropyl)-8-hydro-
xy-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5--
yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate-
: Prep-HPLC condition: (column: Waters Xbridge 150.times.25 mm, 5
.mu.m; liquid phase: [A-10 mM NH.sub.4HCO.sub.3 in H.sub.2O;
B-ACN]B %: 25%-45%, 12 min]). The mixture was concentrated to about
15 mL, and dried by lyophilizer to give
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-(3-(ethylamino)-3-oxopropyl)-8-hydroxy-4,7-
,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((-
7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(89.00 mg, 147.96 umol, 20.58% yield) as white solid. .sup.1H NMR
(DMSO-d.sub.6, 400 MHz) .delta. 9.25 (br. s., 1H), 7.75 (t, J=5.2
Hz, 1H), 7.20 (t, J=8.0 Hz, 1H), 7.10 (d, J=8.0 Hz, 1H), 5.55 (d,
J=8.4 Hz, 1H), 4.92 (s, 2H), 4.80 (s, 2H), 4.43 (d, J=6.2 Hz, 1H),
3.38-3.33 (m, 1H), 3.08-2.98 (m, 2H), 2.27-1.95 (m, 7H), 1.77-1.57
(m, 4H), 1.53-1.22 (m, 9H), 1.07-0.77 (m, 9H), 0.64 (d, J=6.6 Hz,
3H). MS (ESI): mass calcd. for C.sub.32H.sub.45BFNO.sub.8 601.3,
m/z found 602.3 [M+H].sup.+. HPLC: 96.1% in 220 nm; 100% in 254
nm.
[0244]
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-(3-(butylamino)-3-oxopropyl)-8-hydro-
xy-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5--
yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate-
: Prep-HPLC condition: (column: Waters Xbridge 150.times.25 mm, 5
.mu.m; liquid phase: [A-10 mM NH.sub.4HCO.sub.3 in H.sub.2O;
B-ACN]B %: 25%-55%, 12 min]). The mixture was concentrated to about
15 mL, and dried by lyophilizer to give to give
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-(3-(butylamino)-3-oxopropyl)-8-hydroxy-4,7-
,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((-
7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(83.0 mg, 126.1 umol, 23.4% yield, 95.7% purity) as white solid.
.sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 9.24 (br. s., 1H), 7.71
(t, J=5.6 Hz, 1H), 7.23-7.16 (m, 1H), 7.10 (d, J=8.4 Hz, 1H), 5.55
(d, J=8.4 Hz, 1H), 4.92 (s, 1H), 4.80 (s, 1H), 4.43 (d, J=6.2 Hz,
1H), 3.36 (d, J=6.2 Hz, 1H), 3.10-2.91 (m, 2H), 2.25-1.93 (m, 7H),
1.77-1.17 (m, 15H), 0.92-0.77 (m, 9H), 0.64 (d, J=7.1 Hz, 3H). MS
(ESI): mass calcd. for C.sub.34H.sub.49BFNO.sub.8 629.4, m/z found
628.4 [M-H].sup.-. HPLC: 95.67% in 220 nm; 100% in 254 nm.
[0245]
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-(3-(cyclopropylamino)-3-oxopropyl)-8-
-hydroxy-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annu-
len-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)a-
cetate: Prep-HPLC condition: (column: Waters Xbridge 150.times.25
mm, 5 .mu.m; liquid phase: [A-10 mM NH.sub.4HCO.sub.3 in H.sub.2O;
B-ACN]B %: 30%-55%, 12 min]). The mixture was concentrated to about
15 mL, and dried by lyophilizer to give to give
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-(3-(cyclopropylamino)-3-oxopropyl)-8-hydro-
xy-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5--
yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(50.0 mg, 81.5 umol, 6.5% yield) as white solid. .sup.1H NMR
(DMSO-d.sub.6, 400 MHz) .delta. 9.26 (br. s., 1H), 7.82 (d, J=4.0
Hz, 1H), 7.19 (t, J=7.9 Hz, 1H), 7.13-7.08 (m, 1H), 5.55 (d, J=8.0
Hz, 1H), 4.92 (s, 2H), 4.84-4.76 (m, 2H), 4.41 (d, J=6.2 Hz, 1H),
4.02-3.82 (m, 1H), 3.37-3.33 (m, 1H), 2.63-2.54 (m, 2H), 2.26-1.92
(m, 8H), 1.75-1.21 (m, 6H), 1.11-0.76 (m, 8H), 0.69-0.61 (m, 3H),
0.60-0.54 (m, 3H), 0.38-0.31 (m, 3H). MS (ESI): mass calcd. for
C.sub.33H.sub.45BFNO.sub.8 613.3, m/z found 612.3 [M-H].sup.-.
HPLC: 93.1% in 220 nm; 100% in 254 nm.
[0246]
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-7-(3-(3-hydroxypyrrolidin-1--
yl)-3-oxopropyl)-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopent-
a
annulen-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl-
)oxy)acetate: Prep-HPLC condition: ((column: Luna C18 100.times.30
mm, 5 .mu.m; liquid phase: [A-TFA/H.sub.2O=0.075% v/v; B-ACN]B %:
28%-58%, 12 min])). The mixture was dried over lyophilizer to give
to give
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-7-(3-(3-hydroxypyrrolidin-1-yl)-3--
oxopropyl)-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]an-
nulen-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy-
)acetate (72.0 mg, 106.0 umol, 16.8% yield, 94.72% purity) as white
solid. .sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 9.46-9.09 (m,
2H), 7.21 (t, J=8.2 Hz, 1H), 7.10 (d, J=8.0 Hz, 1H), 5.55 (d, J=7.6
Hz, 1H), 4.92 (br. s., 2H), 4.87-4.73 (m, 2H), 4.41 (br. s., 1H),
4.34-4.20 (m, 2H), 3.52 (d, J=4.4 Hz, 2H), 3.42-3.18 (m, 4H),
2.31-1.99 (m, 7H), 1.96-1.21 (m, 15H), 0.95-0.77 (m, 6H), 0.64 (d,
J=6.6 Hz, 3H). MS (ESI): mass calcd. for C.sub.34H.sub.47BFNO.sub.9
643.3, m/z found 642.4 [M-H].sup.-. HPLC: 94.7% in 220 nm; 100% in
254 nm.
[0247]
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-7-(3-((S)-3-hydroxypyrrolidi-
n-1-yl)-3-oxopropyl)-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclo-
penta[8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaboro-
l-6-yl)oxy)acetate: Prep-HPLC condition: (column: Luna C18
100.times.30 mm, 5 .mu.m; liquid phase: [A-TFA/H.sub.2O=0.075% v/v;
B-ACN]B %: 28%-58%, 12 min]). The mixture was dried over
lyophilizer to give to give
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-7-(3-((S)-3-hydroxypyrrolidin-1-yl-
)-3-oxopropyl)-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[-
8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl-
)oxy)acetate: (67.0 mg, 101.6 umol, 16.2% yield, 97.61% purity) as
white solid. .sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 7.21 (t,
J=8.2 Hz, 1H), 7.10 (d, J=8.0 Hz, 1H), 5.55 (d, J=8.0 Hz, 1H), 4.92
(br. s., 2H), 4.86-4.76 (m, 3H), 4.45-4.17 (m, 2H), 3.59-3.46 (m,
2H), 3.42-3.18 (m, 4H), 2.32-1.58 (m, 14H), 1.56-1.21 (m, 8H),
1.08-0.76 (m, 6H), 0.64 (d, J=6.6 Hz, 3H). MS (ESI): mass calcd.
for C.sub.34H.sub.47BFNO.sub.9 643.3, m/z found 642.3 [M-H].sup.-.
HPLC: 97.6% in 220 nm; 100% in 254 nm. [0248] 9.
(3aS,5R,6R,6aR,9aS,10R,10aS,13R)-2-hydroxy-3a,6,10,13-tetramethyl-7-oxodo-
decahydro-6,9a-propanocyclopenta[6,7]cycloocta[1,2-b]furan-5-yl2-((7-fluor-
o-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00119##
[0249] Ozone (51.4 mg, 1.1 mmol, 1.0 eq) was bubbled into a
solution of
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-allyl-3-methoxy-4,7,9,12-tetramethyl-8-oxo-
decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)acetate
(600.0 mg, 1.1 mmol, 1.0 eq) in DCM (50 mL) at -78.degree. C. The
mixture was stirred at -78.degree. C. till TLC showed
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-allyl-3-methoxy-4,7,9,12-tetramethyl-8-oxo-
decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)acetate
consumed, and one new spot was detected. The reaction was quenched
by addition of TEA (1.1 g, 10.7 mmol, 1.5 mL, 10.0 eq) till wet
potassium iodide starch didn't change. The solvent was warmed to
room temperature, and concentrated. The mixture was treated with
DCM (50 mL) and 2N HCl till pH<4. The aqueous phase was treated
with DCM (20 mL.times.3). The combined organic phase was dried over
Na.sub.2SO.sub.4 and concentrated in vacuo to give
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-8-oxo-7-(2-ox-
oethyl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)acetate
(600.0 mg, crude) as yellow oil.
[0250] 7-fluoro-1-hydroxy-3H-2,1-benzoxaborol-6-ol (179.7 mg, 1.1
mmol, 1.0 eq),
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-8-ox-
o-7-(2-oxoethyl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy-
)acetate (600.0 mg, 1.1 mmol, 1.0 eq) and Na.sub.2CO.sub.3 (340.2
mg, 3.2 mmol, 3.0 eq) in DMSO (20 mL) were stirred at 30-40.degree.
C. for 12 hours. HPLC and LCMS showed major as desired. The
reaction was quenched by addition of 50 mL water, and adjusted with
2N HCl till pH<4. White solid was precipitated and filtered to
give crude product
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-8-oxo-7-(2-ox-
oethyl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydro-
xy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (600.0 mg,
crude) as brown solid. MS (ESI): mass calcd. for
C.sub.30H.sub.40BFO.sub.8 558.28, m/z found 557 (M-H).sup.-.
[0251] ZnCl.sub.2 saturated in conc HCl (1.1 mmol, 10.0 mL) was
added to a solution of
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-8-oxo-7-(2-ox-
oethyl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydro-
xy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (600.0 mg, 1.1
mmol, 1.0 eq) in THE (20.0 mL). The mixture was stirred at
20.degree. C. for 4 hours, HPLC showed
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-8-oxo-7-(2-ox-
oethyl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydro-
xy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate consumed, two
new peaks were detected. The mixture was treated with DCM 50 mL and
the aqueous phase was treated with DCM (20 mL.times.2). The
combined organic phase was dried over Na.sub.2SO.sub.4 and
concentrated in vacuo. The crude product was purified by prep-HPLC
(column: Luna C18 100.times.30 mm, 5 .mu.m; liquid phase:
[A-TFA/H.sub.2O=0.075% v/v; B-ACN, B %: 53%-83%, 12 min]). The
mixture was concentrated to about 20 mL solution left and
lyophilized to give
(3aS,5R,6R,6aR,9aS,10R,10aS,13R)-2-hydroxy-3a,6,10,13-tetramethyl-7-oxodo-
decahydro-6,9a-propanocyclopenta[6,7]cycloocta[1,2-b]furan-5-yl2-((7-fluor-
o-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (24.0
mg, 42.0 umol, 3.9% yield) as white solid. .sup.1H NMR
(DMSO-d.sub.6, 400 MHz) .delta. 9.40-9.14 (m, 1H), 7.26-7.19 (m,
1H), 7.12 (d, J=8.0 Hz, 1H), 5.59 (d, J=9.2 Hz, 1H), 5.29 (t, J=6.0
Hz, 1H), 4.92 (s, 2H), 4.88-4.75 (m, 3H), 3.50 (d, J=10.0 Hz, 1H),
2.26-1.94 (m, 6H), 1.76-1.61 (m, 2H), 1.59-1.21 (m, 11H), 1.07-0.92
(m, 5H), 0.68 (d, J=6.4 Hz, 3H). MS (ESI): mass calcd. for
C.sub.29H.sub.38BFO.sub.8 544.26, m/z found 543[M-H].sup.-. HPLC:
95.4% (220 nm), 91.2% (254 nm). [0252] 10.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-benzyl-8-hydroxy-4,7,9,12-tetramethyl-3-ox-
odecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3-
-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00120##
[0253] To a solution of
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-5-(methoxymethoxy)-4,7,9,12-tetram-
ethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one (2.0 g,
5.7 mmol, 1.0 eq) in THE (20 mL) was added NaH (907.2 mg, 22.7
mmol, 60% purity, 4.0 eq) at 0.degree. C. The mixture was stirred
at 50.degree. C. for 1 hr. Then bromomethylbenzene (5.8 g, 34.0
mmol, 4.0 mL, 6.0 eq) was added to the mixture and stirred at
50.degree. C. for 12 hrs. The mixture was cooled to 20.degree. C.
H.sub.2O (60 mL) was added to the mixture. The mixture was
extracted with ethyl acetate (40 mL.times.3). The combined organic
phase was washed with brine (20 mL), dried with anhydrous
Na.sub.2SO.sub.4, filtered and concentrated in vacuum to give a
crude product, which was purified by silica gel chromatography
(Petroleum ether) to afford
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-benzyl-3-methoxy-5-(methoxymethoxy)-4,7,9,-
12-tetramethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one
(2.1 g, 4.7 mmol, 83.7% yield) as white solid.
[0254] To a solution of
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-benzyl-3-methoxy-5-(methoxymethoxy)-4,7,9,-
12-tetramethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one
(2.0 g, 4.5 mmol, 1.0 eq) in MeOH (10.0 mL) was added HCl (2 M,
10.0 mL, 4.4 eq) in one portion at 25.degree. C. The mixture was
stirred at 25.degree. C. for 24 hrs. New peak was detected, but the
starting material was remained by HPLC. H.sub.2O (50 mL) was added
to the mixture, which was extracted with EtOAc (50 mL.times.3). The
combined organic layers were washed with brine (30 mL) and dried
over Na.sub.2SO.sub.4. After filtration via filter paper, the
organic layer was concentrated under reduced pressure to provide a
crude product, which was purified by silica gel chromatography
(petroleum ether/ethyl acetate=50/1) to afford
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-benzyl-5-hydroxy-3-methoxy-4,7,9,12-tetram-
ethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one (800.0
mg, 2.0 mmol, 44.4% yield) as light solid. .sup.1H NMR (CDCl.sub.3,
400 MHz) .delta. 7.31 (d, J=7.2 Hz, 2H), 7.27-7.23 (m, 2H), 4.82
(dd, J=6.4, 9.2 Hz, 1H), 3.53-3.43 (m, 1H), 3.30-3.14 (m, 5H),
2.52-2.45 (m, 1H), 2.27-2.18 (m, 1H), 2.15-2.04 (m, 2H), 2.03-1.91
(m, 1H), 1.56 (m, 4H), 1.44 (d, J=6.4 Hz, 2H), 1.30-1.09 (m, 10H),
1.05 (d, J=6.4 Hz, 3H), 0.93 (s, 3H).
[0255] To a solution of
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-benzyl-5-hydroxy-3-methoxy-4,7,9,12-tetram-
ethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one (804.6
mg, 2.0 mmol, 1.0 eq) and perfluorophenyl 2-(tosyloxy)acetate (2.4
g, 6.1 mmol, 3.0 eq) in THE (25.0 mL) was added DMAP (493.3 mg, 4.0
mmol, 2.0 eq) at 25.degree. C. The mixture was stirred at
25.degree. C. for 18 hrs. H.sub.2O (60 mL) was added the mixture.
The aqueous layer was extracted with EtOAc (30 mL.times.3). The
combined organic layers were washed with brine (20 mL) and dried
over Na.sub.2SO.sub.4. After filtration via filter paper, the
organic layer was concentrated under reduced pressure to provide a
crude product, which was purified by silica gel chromatography
(petroleum ether/ethyl acetate=5/1) to afford
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-benzyl-3-methoxy-4,7,9,12-tetramethyl-8-ox-
odecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)acetate
(600.0 mg, 982.3 umol, 48.6% yield) as a light yellow solid.
.sup.1H NMR (CDCl.sub.3, 400 MHz) .delta. 7.87 (d, J=8.0 Hz, 2H),
7.38-7.29 (m, 2H), 7.26-7.18 (m, 3H), 7.07 (d, J=6.4 Hz, 2H), 6.12
(d, J=10.0 Hz, 1H), 4.82 (dd, J=6.4, 9.5 Hz, 1H), 4.61 (s, 2H),
3.76 (t, J=6.4 Hz, 3H), 3.54-3.36 (m, 2H), 3.11-2.98 (m, 2H),
2.39-2.16 (m, 3H), 2.05 (br. s., 2H), 1.87 (m, 3H), 1.62-1.42 (m,
9H), 1.05 (d, J=6.4 Hz, 2H), 1.01 (d, J=6.4 Hz, 3H), 0.78 (d, J=7.2
Hz, 3H).
[0256] To a solution of
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-benzyl-3-methoxy-4,7,9,12-tetramethyl-8-ox-
odecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)acetate
(600.0 mg, 982.3 umol, 1.1 eq) in DMSO (10.0 mL) was added
Na.sub.2CO.sub.3 (94.7 mg, 893.0 umol, 1.0 eq), KI (148.2 mg, 893.0
umol, 1.0 eq) and 7-fluorobenzo[c][1,2]oxaborole-1,6(3H)-diol at
25.degree. C. under N.sub.2. The reaction mixture was stirred at
25.degree. C. for 5 hrs. H.sub.2O (80 mL) was added the mixture,
which was acidified with aqueous HCl (2 M) till pH=5-6 to
precipitate a white solid. The reaction mixture was filtered and
the filter cake was washed with H.sub.2O (20 mL.times.4) to give a
white solid, which was dissolved in DCM (20 mL) and dried over
Na.sub.2SO.sub.4. After filtration via filter paper, the organic
layer was concentrated under reduced pressure to provide
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-benzyl-3-methoxy-4,7,9,12-tetramethyl-8-ox-
odecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydroxyl-1,-
3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (500.0 mg, crude)
as a light yellow solid.
[0257] To a mixture of
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-benzyl-3-methoxy-4,7,9,12-tetramethyl-8-ox-
odecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3-
-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (500.0 mg, 824.4
umol, 1.0 eq) in THE (5.0 mL) was added ZnCl.sub.2 (10.0 mL
saturated in con.HCl) in one portion at 25.degree. C. The mixture
was stirred at 25.degree. C. for 15 hrs. HPLC and LCMS showed the
reaction was complete. The mixture was added H.sub.2O (20 mL). The
aqueous phase was extracted with DCM (20 mL.times.3). The combined
organic phase was washed with brine (10 mL.times.2), dried with
anhydrous Na.sub.2SO.sub.4, filtered and concentrated in vacuum to
give crude product, which was purified by prep-HPLC (column: Luna
C18 100.times.30 mm, 5 .mu.m; liquid phase: [A-TFA/H.sub.2O=0.075%
v/v; B-ACN]B %: 45%-75%, 12 min]). After prep-HPLC purification,
the eluent was concentrated to remove organic solvent. The residual
aqueous solution was lyophilized to give product
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-benzyl-8-hydroxy-4,7,9,12-tetramethyl-3-ox-
odecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3-
-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (130.0 mg, 214.5
umol, 26.0% yield, 97.8% purity) as white solid. .sup.1H NMR
(DMSO-d.sub.6, 400 MHz) .delta. 7.37-7.29 (m, 1H), 7.21-7.08 (m,
4H), 7.05 (d, J=8.0 Hz, 1H), 6.95 (d, J=7.2 Hz, 2H), 5.92 (d, J=8.4
Hz, 1H), 4.99-4.83 (m, 4H), 2.80-2.73 (m, 2H), 2.39 (br. s., 1H),
2.26-2.00 (m, 4H), 1.85-1.58 (m, 3H), 1.55-1.44 (m, 2H), 1.37-1.11
(m, 6H), 1.08-0.97 (m, 1H), 0.94-0.81 (m, 4H), 0.67 (d, J=5.6 Hz,
3H), 0.55 (s, 3H). MS (ESI): mass calcd. for
C.sub.34H.sub.42BFO.sub.7 592.5, m/z found 591.3 [M-H].sup.-. HPLC:
97.75% (220 nm), 100% (254 nm). [0258] 11.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-(chloromethyl)-8-hydroxy-4,7,9,12-tetramet-
hyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hyd-
roxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00121##
[0259] KHMDS (1M, 51.1 mL, 6.0 eq) was added to a solution of
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-5-(methoxymethoxy)-4,7,9,12-tetram-
ethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one (3.0 g,
8.5 mmol, 1.0 eq) in THE (20 mL) at -78.degree. C., half an hour
later chloro(iodo)methane (7.5 g, 42.6 mmol, 3.1 mL, 5.0 eq) was
added to the mixture and stirred at 25.degree. C. for 12 hrs. The
reaction was quenched by addition of 100 mL water, and treated with
EtOAc (30 mL.times.3). The combined organic phase was dried over
Na.sub.2SO.sub.4 and concentrated in vacuo. The crude product was
purified by flash column chromatography (Petroleum
ether:EtOAc)=100:1 to give
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-(chloromethyl)-3-methoxy-5-(methoxymethoxy-
)-4,7,9,12-tetramethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one
(2.4 g, 6.0 mmol, 70.3% yield) as yellow solid. .sup.1H NMR
(CDCl.sub.3, 400 MHz) .delta. 4.75 (d, J=6.4 Hz, 1H), 4.69 (d,
J=6.4 Hz, 1H), 4.34 (d, J=9.6 Hz, 1H), 4.16 (d, J=11.6 Hz, 1H),
3.60 (d, J=11.6 Hz, 1H), 3.47 (m, 1H), 3.41-3.38 (m, 3H), 3.22 (s,
3H), 3.04 (q, J=6.5 Hz, 1H), 2.48 (dd, J=9.6, 16.0 Hz, 1H),
2.29-2.19 (m, 1H), 2.08-1.93 (m, 3H), 1.89 (d, J=16.0 Hz, 1H), 1.69
(d, J=11.2 Hz, 1H), 1.52 (d, J=4.0 Hz, 2H), 1.40-1.09 (m, 9H), 1.06
(d, J=6.4 Hz, 3H), 0.96 (d, J=7.2 Hz, 3H).
[0260]
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-(chloromethyl)-3-methoxy-5-(methoxym-
ethoxy)-4,7,9,12-tetramethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9-
H)-one (1.0 g, 2.5 mmol, 1.0 eq) in HCl (2M, 218.4 uL, 2.5 eq) and
MeOH (100 mL) were stirred at 15.degree. C. for 12 hour. The
mixture was treated with DCM (100 mL) and water 100 mL. The aqueous
phase was treated with DCM (50 mL.times.2). The combined organic
phase was dried over Na.sub.2SO.sub.4 and concentrated in vacuo.
The crude product was purified by flash column chromatography
(petroleum ether/EtOAc=20/1-5/1) to give
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-(chloromethyl)-5-hydroxy-3-methoxy-
-4,7,9,12-tetramethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one
(800.0 mg, 2.2 mmol, 90.0% yield) as white solid. .sup.1H NMR
(CDCl.sub.3, 400 MHz) .delta. 4.58 (dd, J=9.6, 6.0 Hz, 1H), 4.06
(d, J=11.6 Hz, 1H), 3.63 (d, J=11.6 Hz, 1H), 3.38-3.50 (m, 1H),
3.22 (s, 3H), 3.01 (q, J=6.8 Hz, 1H), 2.50 (dd, J=15.2, 9.6 Hz,
1H), 2.20-2.29 (m, 1H), 1.93-2.09 (m, 2H), 1.65-1.78 (m, 3H), 1.53
(d, J=5.2 Hz, 2H), 1.26-1.20 (m, 4H), 1.21 (s, 3H), 1.14 (s, 3H),
1.08 (d, J=7.2 Hz, 3H), 1.04 (d, J=6.4 Hz, 3H).
[0261]
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-(chloromethyl)-5-hydroxy-3-methoxy-4-
,7,9,12-tetramethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one
(800.0 mg, 2.2 mmol, 1.0 eq), perfluorophenyl 2-(tosyloxy)acetate
(1.2 g, 2.9 mmol, 1.3 eq) and DMAP (273.8 mg, 2.2 mmol, 1.0 eq) in
THE (15 mL) were stirred at 20.degree. C. for 12 hr. The solvent
was concentrated in vacuo directly. The crude product was purified
by flash column chromatography (P etroleum ether/EtOAc=I/O-5/1) to
give
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-(chloromethyl)-3-methoxy-4,7,9,12-tetramet-
hyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)acetat-
e (850.0 mg, 1.5 mmol, 66.7% yield) as yellow iol. .sup.1H NMR
(CDCl.sub.3, 400 MHz) .delta. 7.85 (d, J=8.4 Hz, 2H), 7.38 (d,
J=8.4 Hz, 2H), 5.74 (d, J=10.0 Hz, 1H), 4.62-4.56 (m, 1H), 4.54 (s,
2H), 4.37 (d, J=12.0 Hz, 1H), 3.39 (d, J=11.6 Hz, 2H), 3.23-3.18
(m, 3H), 3.05 (d, J=6.0 Hz, 1H), 2.54 (dd, J=10.0, 16.0 Hz, 1H),
2.48 (s, 3H), 2.30-2.20 (m, 1H), 2.09-1.93 (m, 3H), 1.72 (d, J=11.2
Hz, 1H), 1.56-1.44 (m, 3H), 1.38-1.19 (m, 8H), 1.17 (s, 3H), 1.07
(d, J=6.4 Hz, 3H), 0.74 (d, J=7.2 Hz, 3H).
[0262] Na.sub.2CO.sub.3 (419.0 mg, 4.0 mmol, 3.0 eq) was added to a
solution of
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-(chloromethyl)-3-methoxy-4,7,9,12-tetramet-
hyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)acetat-
e (750.0 mg, 1.3 mmol, 1.0 eq) and
7-fluoro-1-hydroxy-3H-2,1-benzoxaborol-6-ol (221.3 mg, 1.3 mmol,
1.0 eq) in DMSO (20 mL). The mixture was stirred at 30.degree. C.
for 12 hrs. The reaction was quenched by addition of 50 mL water,
and adjusted by addition of 2N HCl untill pH<4, white solid was
precipitated and filtered to give crude product to give
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-(chloromethyl)-3-methoxy-4,7,9,12-tetramet-
hyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hyd-
roxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (710.0 mg,
crude) as yellow solid.
[0263] ZnCl.sub.2 saturated in Con HCl (1.2 mmol, 15.0 mL, 1.0 eq)
was added to a solution of
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-(chloromethyl)-3-methoxy-4,7,9,12-tetramet-
hyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hyd-
roxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (700.0 mg,
1.2 mmol, 1.0 eq) in THE (20 mL) at 20.degree. C. for 12 hrs. The
reaction was treated with water 50 mL and 50 mL DCM. The aqueous
solution was treated with DCM (30 mL.times.3). The combined organic
phase was dried over Na.sub.2SO.sub.4 and concentrated in vacuo.
The crude product was purified by prep-HPLC (column: Luna C18
100.times.30 mm, 5 .mu.m; liquid phase: [A-TFA/H.sub.2O=0.075% v/v;
B-ACN, B %: 30%-60%, 12 min]). The solvent was concentrated to 30
mL solution left and lyophilized to give
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-(chloromethyl)-8-hydroxy-4,7,9,12-tetramet-
hyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hyd-
roxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (226.00 mg,
410.28 umol, 33.09% yield, 100% purity) as white solid. .sup.1H NMR
(DMSO-d.sub.6, 400 MHz) .delta. 9.13 (s, 1H), 7.21 (t, J=8.0 Hz,
1H), 7.07 (d, J=8.0 Hz, 1H), 5.65 (d, J=8.0 Hz, 1H), 4.92 (s, 2H),
4.87-4.73 (m, 2H), 3.89 (d, J=11.2 Hz, 1H), 3.72 (d, J=10.4 Hz,
1H), 3.55 (d, J=6.4 Hz, 1H), 2.41 (s, 1H), 2.24-1.99 (m, 3H), 1.88
(dd, J=8.0, 16.8 Hz, 1H), 1.73-1.22 (m, 12H), 1.02 (s, 3H), 0.82
(d, J=6.4 Hz, 3H), 0.64 (d, J=7.2 Hz, 3H). MS (ESI): mass calcd.
for C.sub.28H.sub.37BClFO.sub.7550.23, m/z found 549.4(M-H).sup.-.
HPLC: 100% (220 nm), 100% (254 nm). [0264] 12. methyl
(E)-3-((3aR,4R,5R,7S,8S,9R,9aS,12R)-5-(2-((7-fluoro-1-hydroxy-1,3--
dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetoxy)-8-hydroxy-4,7,9,12-tetramet-
hyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-7-yl)acrylate
[0265] 13.
(E)-3-((3aR,4R,5R,7S,8S,9aS,12R)-5-(2-((7-fluoro-1-hydroxy-1,3-dihydr-
obenzo[c][1,2]oxaborol-6-yl)oxy)acetoxy)-8-hydroxy-4,7,12-trimethyl-3-oxod-
ecahydro-4,9a-propanocyclopenta[8]annulen-7-yl)acrylic acid
##STR00122##
[0266]
(E)-methyl3-((3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetram-
ethyl-3-oxo-5-(2-(tosyloxy)acetoxy)decahydro-4,9a-propanocyclopenta[8]annu-
len-7-yl)acrylate (400.0 mg, 677.1 umol, 1.0 eq),
7-fluoro-1-hydroxy-3H-2,1-benzoxaborol-6-ol (113.7 mg, 677.1 umol,
1.0 eq) and Na.sub.2CO.sub.3 (215.3 mg, 2.0 mmol, 3.0 eq) in DMSO
(10.0 mL) were heated to 30-40.degree. C. for 12 hours. Water (30
mL) was added to the mixture, white solid was precipitated. The
mixture was filtered to give crude product, which was purified by
prep-HPLC (column: Luna C18 100.times.30 mm, 5 .mu.m; liquid phase:
[A-TFA/H.sub.2O=0.075% v/v; B-ACN]B %: 42%-57%, 12 min]). The
mixture was concentrated to about 20 mL solution left and dried
over lyophilizer to give
(E)-methyl3-((3aR,4R,5R,7S,8S,9R,9aS,12R)-5-(2-((7-fluoro-1-hydroxy-1,3-d-
ihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetoxy)-8-hydroxy-4,7,9,12-tetrameth-
yl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-7-yl)acrylate
(126.0 mg, 214.8 umol, 31.7% yield, 100% purity) as white solid and
53 mg delivered. .sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 7.21
(t, J=8.2 Hz, 1H), 7.12-7.04 (m, 2H), 5.70 (d, J=16.3 Hz, 1H), 5.56
(d, J=7.9 Hz, 1H), 4.91 (d, J=1.8 Hz, 2H), 4.86-4.75 (m, 2H), 3.65
(s, 3H), 2.25-1.96 (m, 4H), 1.76-1.19 (m, 10H), 1.16-0.92 (m, 5H),
0.89-0.74 (m, 6H), 0.64 (d, J=6.6 Hz, 3H). MS (ESI): mass calcd.
for C.sub.31H.sub.40BFP.sub.9 586.3, m/z found 585.3 [M-H].sup.-.
HPLC: 99.9% in 220 nm; 100% in 254 nm.
[0267]
(E)-methyl3-((3aR,4R,5R,7S,8S,9R,9aS,12R)-5-(2-((7-fluoro-1-hydroxy-
-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetoxy)-8-hydroxy-4,7,9,12-tet-
ramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-7-yl)acrylate
(73.0 mg, 124.5 umol, 1.0 eq) and LiOHH.sub.2O (10.4 mg, 249.0
umol, 2.0 eq) in MeOH (5.0 mL) and H.sub.2O (5.0 mL) were stirred
at 15.degree. C. for 12 hours. 10 mL water was added to the
mixture, the aqueous phase was adjusted to pH<5, white solid was
precipitated. The mixture was filtered to give crude product, which
was purified by prep-HPLC (column: Luna C18 100.times.30 mm, 5
.mu.m; liquid phase: [A-TFA/H.sub.2O=0.075% v/v; B-ACN]B %:
32%-47%, 15 min]), the mixture was concentrated to about 15 mL
solution left. The product was dried over lyophilizer to give
(E)-3-((3aR,4R,5R,7S,8S,9R,9aS,12R)-5-(2-((7-fluoro-1-hydroxy-1,3-dihydro-
benzo[c][1,2]oxaborol-6-yl)oxy)acetoxy)-8-hydroxy-4,7,9,12-tetramethyl-3-o-
xodecahydro-4,9a-propanocyclopenta[8]annulen-7-yl)acrylic acid
(21.0 mg, 36.2 umol, 29.1% yield, 98.7% purity) as white solid.
.sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 9.26 (s, 1H), 7.24-7.18
(m, 1H), 7.09 (d, J=8.4 Hz, 1H), 6.99 (d, J=16.3 Hz, 1H), 5.61 (d,
J=16 Hz, 1H), 5.56 (d, J=8.4 Hz, 1H), 4.91 (s, 2H), 4.88-4.76 (m,
2H), 4.58 (d, J=6.2 Hz, 1H), 3.62 (t, J=6.4 Hz, 1H), 2.26-2.00 (m,
4H), 1.76-1.22 (m, 11H), 1.08 (s, 4H), 0.87-0.78 (m, 4H), 0.64 (d,
J=7.1 Hz, 3H). MS (ESI): mass calcd. for C.sub.30H.sub.38BFP.sub.9
572.3, m/z found 571.3 [M-H].sup.-. HPLC: 98.7% in 220 nm; 100% in
254 nm. [0268] 14.
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-((E)-3-amino-3-oxoprop-1-en-1-yl)-8-hydrox-
y-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-y-
l2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00123##
[0269] To a mixture of
(E)-3-((3aR,4R,5R,7S,8S,9R,9aS,12R)-5-(2-((7-fluoro-1-hydroxy-1,3-dihy
drobenzo[c][1,2]oxaborol-6-yl)oxy)acetoxy)-8-hydroxy-4,7,9,12-tetramethyl-
-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-7-yl)acrylic acid
(0.4 g, 700.0 umol, 1.0 eq), HATU (0.3 g, 768.7 umol, 1.1 eq) and
TEA (141.4 mg, 1.4 mmol, 2.0 eq) in DMF (5.0 mL) was added
ammonia;hydrochloride (74.8 mg, 1.4 mmol, 2.0 eq) in one portion at
25.degree. C. The mixture was stirred at 25.degree. C. for 4 hours.
HPLC and LCMS showed the reaction was complete. The mixture was
added H.sub.2O (10 mL). The aqueous phase was acidified with
aqueous HCl (2M) till pH=3-4 and extracted with DCM (15
mL.times.3). The combined organic layers were washed with saturated
brine (10 mL) and dried over Na.sub.2SO.sub.4. The organic layer
was filtered and concentrated under reduced pressure to provide
crude product, which was purified by prep-HPLC (column: Phenomenex
luna C18 130.times.25 mm, 5 .mu.m; liquid phase: [A: 10 mM
NH.sub.4HCO.sub.3 in H.sub.2O; B-ACN]B %: 20%-45%, 12 min]). After
prep-HPLC purification, the eluent was concentrated to remove
organic solvents. The residual aqueous solution was lyophilized to
give
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-((E)-3-amino-3-oxoprop-1-en-1-yl)-8-hydrox-
y-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-y-
l2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(100.0 mg, 173.9 umol, 24.9% yield) as a white solid. .sup.1H NMR
(DMSO-d.sub.6, 400 MHz) .delta. 9.28 (s, 1H), 7.28 (br. s., 1H),
7.21 (t, J=8.0 Hz, 1H), 7.06-7.15 (m, 1H), 6.72-6.86 (m, 2H), 5.76
(d, J=15.6 Hz, 1H), 5.58 (d, J=8.0 Hz, 1H), 4.92 (s, 2H), 4.78-4.86
(m, 2H), 4.51 (d, J=6.0 Hz, 1H), 3.56-3.62 (m, 1H), 2.00-2.26 (m,
3H), 1.47-1.74 (m, 4H), 1.22-1.46 (m, 6H), 1.00-1.13 (m, 4H),
0.89-0.96 (m, 2H), 0.82 (d, J=7.0 Hz, 3H), 0.65 (d, J=6.4 Hz, 3H).
MS (ESI): mass calcd. for C.sub.30H.sub.39BFNO.sub.8 571.44, m/z
found 570.3 [M-H].sup.-. HPLC: 99.4% (220 nm), 100% (254 nm).
[0270] 15.
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-((E)-3-(met-
hylamino)-3-oxoprop-1-en-1-yl)-3-oxodecahydro-4,9a-propanocyclopenta[8]ann-
ulen-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)-
acetate
##STR00124##
[0271] To a mixture of
(E)-3-((3aR,4R,5R,7S,8S,9R,9aS,12R)-5-(2-((7-fluoro-1-hydroxy-1,3-dihy
drobenzo[c][1,2]oxaborol-6-yl)oxy)acetoxy)-8-hydroxy-4,7,9,12-tetramethyl-
-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-7-yl)acrylic acid
(300.0 mg, 524.1 umol, 1.0 eq), HATU (219.2 mg, 576.5 umol, 1.1 eq)
and TEA (106.1 mg, 1.1 mmol, 2.0 eq) in DMF (5 mL) was added
methanamine;hydrochloride (70.8 mg, 1.1 mmol, 2.0 eq) in one
portion at 25.degree. C. The mixture was stirred at 25.degree. C.
for 4 hours. HPLC and LCMS showed the reaction was complete. The
mixture was added H.sub.2O (10 mL). The aqueous phase was acidified
with aqueous HCl (2M) till pH=3-4 and extracted with DCM (15
mL.times.3). The combined organic layers were washed with saturated
brine (10 mL) and dried over Na.sub.2SO.sub.4. The organic layer
was filtered and concentrated under reduced pressure to provide
crude product, which and ET5616-20-P1 (110 mg) were combined and
purified by prep-HPLC (column: Phenomenex luna C18 130.times.25 mm,
5 .mu.m; liquid phase: [A A-10 mM NH.sub.4HCO.sub.3 in H.sub.2O;
B-ACN]B %:20%-45%, 12 min]). After prep-HPLC purification, the
eluent was concentrated to remove organic solvents. The residual
aqueous solution was lyophilized to give
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-((E)-3-(met-
hylamino)-3-o
xoprop-1-en-1-yl)-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(-
(7-fluoro-1-hy droxy-1,3-dihydrobe
nzo[c][1,2]oxaborol-6-yl)oxy)acetate (280.0 mg) as a white solid.
.sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 7.78 (d, J=4.4 Hz, 1H),
7.20 (t, J=8.0 Hz, 1H), 7.05-7.15 (m, 1H), 6.76 (d, J=16.0 Hz, 1H),
5.74 (d, J=16.0 Hz, 1H), 5.57 (d, J=8.0 Hz, 1H), 4.89-4.96 (m, 2H),
4.76-4.86 (m, 2H), 4.49 (d, J=6.0 Hz, 1H), 3.59 (t, J=6.0 Hz, 1H),
2.64 (d, J=4.4 Hz, 3H), 2.01-2.26 (m, 4H), 1.48-1.72 (m, 4H),
1.23-1.43 (m, 6H), 1.01-1.11 (m, 3H), 0.88-0.95 (m, 1H), 0.82 (d,
J=6.4 Hz, 3H), 0.62-0.68 (d, J=7.0 Hz, 3H). MS (ESI): mass calcd.
for C.sub.31H.sub.41BFNO.sub.8 585.47, m/z found 584.3 [M-H].sup.-.
HPLC: 99.3% (220 nm), 100% (254 nm). [0272] 16.
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-7-((E)-3-(methoxyamino)-3-oxoprop--
1-en-1-yl)-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]an-
nulen-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy-
)acetate
##STR00125##
[0273] To a mixture of (E)-methyl
3-((3aR,4R,5R,7S,8S,9R,9aS,12R)-5-(2-((7-fluoro-1-hydroxy-1,3-dihydrobenz-
o[c][1,2]oxaborol-6-yl)oxy)acetoxy)-8-hydroxy-4,7,9,12-tetramethyl-3-oxode-
cahydro-4,9a-propanocyclopenta[8]annulen-7-yl)acrylate (8.0 g, 13.6
mmol, 1.0 eq) in MeOH (30 mL) and H.sub.2O (40 mL) was added LiOH
H.sub.2O (1.1 g, 27.3 mmol, 2.0 eq) in one portion at 20.degree. C.
The mixture was stirred at 20.degree. C. for 5 hours. HPLC showed
the reaction was complete. H.sub.2O (30 mL) was added to the
mixture which was acidified with aqueous HCl (2 M) till pH=5-6 to
precipitate a white solid. The aqueous layer was extracted with
EtOAc (50 mL.times.3). The combined organic layers were washed with
brine (20 mL) and dried over Na.sub.2SO.sub.4. After filtration via
filter paper, the organic layer was concentrated under reduced
pressure to provide a crude product, which was purified by
prep-HPLC (column: Phenomenex luna C18 250.times.50 mm, 10 .mu.m;
liquid phase: [A-TFA/H.sub.2O=0.075% v/v; B-ACN]B %: 25%-55%, 20
min]). After prep-HPLC purification, the eluent was concentrated to
remove organic solvent. The residual aqueous solution was
lyophilized to give
(E)-3-((3aR,4R,5R,7S,8S,9R,9aS,12R)-5-(2-((7-fluoro-1-hydroxy-1,3-di-
hydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetoxy)-8-hydroxy-4,7,9,12-tetramethy-
l-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-7-yl)acrylic acid
(3.0 g, 5.2 mmol, 38.4% yield) as a white solid.
[0274] To a mixture of
(E)-3-((3aR,4R,5R,7S,8S,9R,9aS,12R)-5-(2-((7-fluoro-1-hydroxy-1,3-dihy
drobenzo[c][1,2]oxaborol-6-yl)oxy)acetoxy)-8-hydroxy-4,7,9,12-tetramethyl-
-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-7-yl)acrylic acid
(200.0 mg, 349.4 umol, 1.0 eq), HATU (146.1 mg, 384.3 umol, 1.1
eq), TEA (70.7 mg, 698.8 umol, 2.0 eq) in DMF (10.0 mL) was added
O-methylhydroxylamine hydrochloride (58.4 mg, 698.8 umol, 2.0 eq)
in one portion at 25.degree. C. The mixture was stirred at
25.degree. C. for 3 hours. HPLC showed the reaction was completed.
H.sub.2O (30 mL) was added the mixture, which was acidified with
aqueous HCl (2 M) till pH=5-6 to precipitate a white solid. The
aqueous layer was extracted with EtOAc (20 mL.times.3). The
combined organic layers were washed with brine (20 mL) and dried
over Na.sub.2SO.sub.4. After filtration via filter paper, the
organic layer was concentrated under reduced pressure to provide
crude product, which was purified by prep-HPLC (column: Luna C18
100.times.30 mm, 5 .mu.m; liquid phase: [A: TFA/H.sub.2O=0.075%
v/v; B-ACN]B %: 35%-65%, 12 min]). After prep-HPLC purification,
the eluent was concentrated to remove organic solvent. The residual
aqueous solution was lyophilized to give
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-7-((E)-3-(methoxyamino)-3-oxoprop--
1-en-1-yl)-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]an-
nulen-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy-
)acetate (75.0 mg, 118.1 umol, 33.8% yield) as a white solid.
.sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 7.17 (t, J=8.0 Hz, 1H),
7.05 (d, J=8.0 Hz, 1H), 6.83 (d, J=16.0 Hz, 1H), 5.52 (d, J=8.4 Hz,
2H), 4.88 (s, 2H), 4.71-4.84 (m, 2H), 3.57 (s, 5H), 1.96-2.21 (m,
5H), 1.64 (d, J=12.4 Hz, 2H), 1.39-1.53 (m, 2H), 1.19-1.38 (m, 6H),
0.86-1.09 (m, 5H), 0.77 (d, J=7.2 Hz, 3H), 0.61 (d, J=6.6 Hz, 3H).
MS (ESI): mass calcd. for C.sub.31H.sub.41BFNO.sub.9 601.29, m/z
found 602.4 [M+H].sup.+. HPLC: 94.7% (220 nm), 94.2% (254 nm).
[0275] 17. tert-butyl
2-((E)-3-((3aR,4R,5R,7S,8S,9R,9aS,12R)-5-(2-((7-fluoro-1-hydroxy-1,3-dihy-
drobenzo[c][1,2]oxaborol-6-yl)oxy)acetoxy)-8-hydroxy-4,7,9,12-tetramethyl--
3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-7-yl)acryloyl)hydrazine-1--
carboxylate [0276] 18.
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-((E)-3-hydrazinyl-3-oxoprop-1-en-1-yl)-8-h-
ydroxy-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annule-
n-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)ace-
tate
##STR00126##
[0277] To a mixture of
(E)-3-((3aR,4R,5R,7S,8S,9R,9aS,12R)-5-(2-((7-fluoro-1-hydroxy-1,3-dihydr
obenzo[c][1,2]oxaborol-6-yl)oxy)acetoxy)-8-hydroxy-4,7,9,12-tetramethyl-3-
-oxodecahydro-4,9a-propanocyclopenta[8]annulen-7-yl)acrylic acid
(1.0 g, 1.7 mmol, 1.0 eq), HATU (731.9 mg, 1.9 mmol, 1.1 eq) and
TEA (354.2 mg, 3.5 mmol, 2.0 eq) in DMF (20 mL) was added
tert-butyl N-aminocarbamate (462.6 mg, 3.5 mmol, 2.0 eq) in one
portion at 25.degree. C. The mixture was stirred at 25.degree. C.
for 3 hours. HPLC showed the reaction was completed. H.sub.2O (100
mL) was added the mixture, which was acidified with aqueous HCl (2
M) till pH=5-6 to precipitate a white solid. The aqueous layer was
extracted with EtOAc (50 mL.times.3). The combined organic layers
were washed with brine (30 mL) and dried over Na.sub.2SO.sub.4.
After filtration via filter paper, the organic layer was
concentrated under reduced pressure to provide crude product, which
was purified by prep-HPLC (column: Phenomenex luna C18 130.times.25
mm, 5 .mu.m; liquid phase: [A-10 mM NH.sub.4HCO.sub.3 in H.sub.2O;
B-ACN]B %: 20%-55%, 12 min]). After prep-HPLC purification, the
eluent was concentrated to remove organic solvents. The residual
aqueous solution was lyophilized to give tert-butyl
2-((E)-3-((3aR,4R,5R,7S,8S,9R,9aS,12R)-5-(2-((7-fluoro-1-hydroxy-1,3-dihy-
drobenzo[c][1,2]oxaborol-6-yl)oxy)acetoxy)-8-hydroxy-4,7,9,12-tetramethyl--
3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-7-yl)acryloyl)hydrazinecar-
boxylate (160.0 mg, 224.5 umol, 12.8% yield) as a white solid.
.sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 9.45 (br. s., 1H), 9.22
(s, 1H), 8.71 (br. s., 1H), 7.12-7.20 (m, 1H), 7.03-7.10 (m, 1H),
6.85 (d, J=16.0 Hz, 1H), 5.73 (d, J=15.4 Hz, 1H), 5.53 (d, J=7.6
Hz, 1H), 4.88 (s, 2H), 4.72-4.85 (m, 2H), 4.52 (d, J=6.2 Hz, 1H),
3.54-3.62 (m, 1H), 1.99-2.21 (m, 3H), 1.55-1.70 (m, 2H), 1.17-1.51
(m, 18H), 0.88-1.13 (m, 5H), 0.76-0.82 (d, J=7.2 Hz, 3H), 0.61 (d,
J=7.2 Hz, 3H). MS (ESI): mass calcd. for
C.sub.35H.sub.48BFN.sub.2O.sub.10 686.34, m/z found 685.4
[M-H].sup.-. HPLC: 96.3% (220 nm), 100% (254 nm).
[0278] To a solution of tert-butyl
2-((E)-3-((3aR,4R,5R,7S,8S,9R,9aS,12R)-5-(2-((7-fluoro-1-hy
droxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetoxy)-8-hydroxy-4,7,9,-
12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-7-yl)acrylo-
yl)hydrazinecarboxylate (1.0 g, 1.5 mmol, 1.0 eq) in DCM was added
HCl/EtOAc (4 M, 80.2 mL, 219.7 eq) at 25.degree. C. The mixture was
stirred at 25.degree. C. for 3.5 hours. HPLC showed the reaction
was complete. The reaction mixture was filtered and the filter cake
was washed with 20 mL of ethyl acetate, dried in vacuum to give or
afford product, which was purified by prep-HPLC (column: Luna C18
100.times.30 mm, 5 .mu.m; liquid phase: [A-HCl/H.sub.2O=0.040% v/v;
BACN]B %: 25%-55%, 12 min]). After prep-HPLC purification, the
eluent was concentrated to remove organic solvents. The residual
aqueous solution was lyophilized to give
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-((E)-3-hydrazinyl-3-oxoprop-1-en-1-yl-
)-8-hydroxy-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]a-
nnulen-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxa
borol-6-yl)oxy)acetate (76.0 mg, 120.9 umol, 8.3% yield) as a white
solid. .sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 10.68 (br. s.,
1H), 9.24 (br. s., 1H), 7.13-7.21 (m, 1H), 7.07 (d, J=8.4 Hz, 1H),
6.98 (d, J=16.0 Hz, 1H), 5.81 (d, J=16.0 Hz, 1H), 5.53 (d, J=8.0
Hz, 1H), 4.88 (s, 2H), 4.71-4.84 (m, 2H), 3.62 (d, J=5.6 Hz, 1H),
2.55-2.50 (m, 1H), 2.42 (d, J=1.8 Hz, 1H), 1.96-2.23 (m, 4H),
1.57-1.77 (m, 2H), 1.40-1.52 (m, 1H), 1.19-1.40 (m, 7H), 0.93-1.14
(m, 5H), 0.78 (d, J=7.2 Hz, 3H), 0.61 (d, J=7.2 Hz, 3H). MS (ESI):
mass calcd. for C.sub.30H.sub.41BClFN.sub.2O.sub.8 622.92, m/z
found 585.3 [M-H].sup.-. HPLC: 99.7% (220 nm), 100% (254 nm).
[0279] 19.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-ethyl-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-
decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3--
dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00127##
[0280]
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-7-
-vinyldecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)acetate
(500.0 mg, 938.6 umol, 1.0 eq) and Pd/C (300.0 mg, 938.6 umol, 1.0
eq) in THE (30.0 mL) were stirred at 25.degree. C. for 12 hours
under 40 psi hydrogen atmosphere. The mixture was filtered and the
filtrate was concentrated to give
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-ethyl-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-
decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)acetate
(500.0 mg, 902.8 umol, 96.2% yield, 96.5% purity) as white foam.
.sup.1H NMR (CHLOROFORM-d, 400 MHz) .delta. 7.83 (d, J=8.4 Hz, 2H),
7.36 (d, J=8.4 Hz, 2H), 5.66 (d, J=7.9 Hz, 1H), 4.51 (s, 2H),
3.45-3.37 (m, 1H), 2.46 (s, 3H), 2.41-2.14 (m, 4H), 2.09 (br. s.,
1H), 1.85-1.05 (m, 15H), 0.99-0.91 (m, 6H), 0.72 (t, J=7.5 Hz, 3H),
0.61 (d, J=7.1 Hz, 2H).
[0281]
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-ethyl-8-hydroxy-4,7,9,12-tetramethyl-
-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)acetate
(300.0 mg, 561.1 umol, 1.0 eq),
7-fluoro-1-hydroxy-3H-2,1-benzoxaborol-6-ol (94.22 mg, 561.06 umol,
1.00 eq) and Na.sub.2CO.sub.3 (178.4 mg, 1.7 mmol, 3.0 eq) in DMSO
(15.0 mL) were heated to 30-40.degree. C. for 12 hours. Water (20
mL) was added to the mixture, white solid was precipitated. The
mixture was filtered to give crude product, which was purified by
prep-HPLC (column: Luna C18 100.times.30 mm, 5 .mu.m; liquid phase:
[A-TFA/H.sub.2O=0.075% v/v; B-ACN]B %: 41%-61%, 12 min]) to give
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-ethyl-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-
decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3--
dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (95.00 mg, 179.10
umol, 31.92% yield, 100% purity) as white solid. .sup.1H NMR
(DMSO-d.sub.6, 400 MHz) .delta. 9.26 (s, 1H), 7.24-7.21 (m, 1H),
7.12-7.06 (m, 1H), 5.58 (d, J=8.4 Hz, 1H), 4.92-4.83 (m, 2H),
4.84-4.80 (m, 2H), 4.40 (d, J=5.6 Hz, 1H), 3.34-3.32 (m, 1H),
2.37-2.18 (m, 1H), 2.24-2.00 (m, 3H), 1.80-0.93 (m, 20H), 0.88-0.77
(m, 3H), 0.66-0.56 (m, 3H). MS (ESI): mass calcd. for
C.sub.29H.sub.40BFO.sub.7 530.3, m/z found 529.3 [M-H].sup.-. HPLC:
100% in 220 nm; 10% in 254 nm. [0282] 20.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-ethyl-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-
decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((4-(aminomethyl)-1-hydro-
xy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00128##
[0283] A solution of
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-7-vinyl-
decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((4-(aminomethyl)-1-hydro-
xy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (40 mg, 0.074
mmol) in MeOH (5 mL) was hydrogenated using Pd/C (10%) (8 mg) as
catalyst under atmospheric pressure for 6 h. The catalyst was
removed by filtration, the solvent was removed and the residue was
purified by Prep-HPLC to give
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-ethyl-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-
decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((4-(aminomethyl)-1-hydro-
xy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (2.6 mg, yield
6.5%) as a white solid. .sup.1H NMR (400 MHz, DMSO-d.sub.6) .delta.
9.02 (s, 1H), 7.07 (s, 1H), 7.04 (s, 1H), 5.58 (d, J=4.8 Hz, 1H),
4.95 (s, 2H), 4.69 (q, J=20.8 Hz, 2H), 4.41 (d, J=6.0 Hz, 1H), 3.64
(s, 2H), 2.42-2.07 (m, 5H), 1.75-1.04 (m, 16H), 0.84-0.79 (m, 6H),
0.65 (d, J=6.8 Hz, 3H), 0.59 (t, J=7.2 Hz, 3H). HPLC purity: 100%
(220 nm), 100% (254 nm); MS (ESI): mass calcd. for
C.sub.30H.sub.44BNO.sub.7 541.32, m/z found 542.5 [M+H].sup.+.
[0284] 21.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-allyl-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-
decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3--
dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00129##
[0285] NaOH (6.1 g, 152.9 mmol, 3.0 eq) was added to a solution of
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-8-oxo-7-vinyl-
decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-hydroxyacetate
(20.0 g, 51.0 mmol, 1.0 eq) in MeOH (100 mL) and H.sub.2O (100 mL)
at 15.degree. C. The mixture was stirred at 15.degree. C. for 12
hours. The solvent was concentrated in vacuo. 100 mL water was
added to the mixture, and treated with EtOAc (100 mL.times.2). The
combined organic phase was dried over Na.sub.2SO.sub.4 and
concentrated in vacuo to give
(3R,3aS,4R,5R,7S,9R,9aR,12R)-5-hydroxy-3-methoxy-4,7,9,12-tetramethyl-7-v-
inyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one (17.0 g,
crude) as brown oil. .sup.1H NMR (CDCl.sub.3, 400 MHz) .delta. 6.01
(dd, J=10.4, 17.6 Hz, 1H), 5.30-5.21 (m, 2H), 4.64 (dd, J=6.0, 9.2
Hz, 1H), 3.49 (m, 1H), 2.93 (q, J=6.4 Hz, 1H), 2.43 (dd, J=9.2,
15.2 Hz, 1H), 2.24-2.15 (m, 1H), 2.05-1.93 (m, 2H), 1.83 (d, J=15.6
Hz, 1H), 1.72 (d, J=11.0 Hz, 1H), 1.64-1.42 (m, 5H), 1.40-1.19 (m,
3H), 1.17 (d, J=7.6 Hz, 7H), 1.08 (d, J=7.2 Hz, 3H), 0.98 (d, J=6.4
Hz, 3H).
[0286] MOMCl (37.3 g, 463.4 mmol, 35.2 mL, 5.0 eq) was added to a
solution of
(3R,3aS,4R,5R,7S,9R,9aR,12R)-5-hydroxy-3-methoxy-4,7,9,12-tetramethyl--
7-vinyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one (31.0
g, 92.7 mmol, 1.0 eq) and DIEA (71.9 g, 556.1 mmol, 97.1 mL, 6.0
eq) in DCM (200.0 mL) at 0.degree. C., the mixture was stirred at
20.degree. C. for 12 hours. The reaction was quenched by addition
of 300 mL water, and adjusted to pH<5 with 2 N HCl and treated
with DCM (100 mL.times.3). The combined organic phase was washed by
brine 100 mL.times.1 and concentrated in vacuo to give
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-5-(methoxymethoxy)-4,7,9,12-tetram-
ethyl-7-vinyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one
(35.0 g, crude) as yellow oil. .sup.1H NMR (CDCl.sub.3, 400 MHz)
.delta. 6.34 (dd, J=10.8, 17.4 Hz, 1H), 5.26 (d, J=11.2 Hz, 1H),
5.05 (d, J=17.6 Hz, 1H), 4.80-4.68 (m, 2H), 4.34 (d, J=9.6 Hz, 1H),
3.50 (m, 1H), 3.43-3.40 (m, 3H), 3.23 (s, 2H), 2.91 (q, J=6.4 Hz,
1H), 2.40 (dd, J=9.6, 15.4 Hz, 1H), 2.24-2.14 (m, 1H), 2.05-1.91
(m, 3H), 1.68 (d, J=11.2 Hz, 1H), 1.57 (s, 3H), 1.48 (d, J=3.2 Hz,
2H), 1.37-1.23 (m, 2H), 1.20 (d, J=4.4 Hz, 6H), 1.16-1.04 (m, 2H),
0.98 (t, J=6.2 Hz, 6H).
[0287] Ozone (4.4 g, 92.5 mmol, 1.0 eq) was bubbled into a solution
of
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-5-(methoxymethoxy)-4,7,9,12-tetram-
ethyl-7-vinyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one
(35.0 g, 92.5 mmol, 1.0 eq) in DCM (2.5 L) at -78.degree. C., the
mixture was stirred at -78.degree. C. till TLC showed that the
starting material was consumed. The reaction was quenched by
addition of TEA (93.6 g, 924.6 mmol, 128.2 mL, 10.0 eq) till wet
potassium iodide starch didn't change. The solvent was warmed to
room temperature, and concentrated. The mixture was treated with
DCM (200 mL) and 2N HCl till pH<4. The aqueous phase was treated
with DCM (100 mL.times.3). The combined organic phase was dried
over Na.sub.2SO.sub.4 and concentrated in vacuo to give
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-5-(methoxymethoxy)-4,7,9,12-tetram-
ethyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulene-7-carbaldehyde
(35.0 g, crude) as yellow oil. .sup.1H NMR (DMSO-d.sub.6, 400 MHz)
.delta. 9.60 (s, 1H), 4.78 (d, J=7.2 Hz, 1H), 4.70 (d, J=7.2 Hz,
1H), 4.23 (d, J=8.0 Hz, 1H), 3.45-3.36 (m, 4H), 3.22 (s, 3H), 2.92
(q, J=6.4 Hz, 1H), 2.52-2.35 (m, 2H), 2.26-2.14 (m, 1H), 2.07-1.87
(m, 2H), 1.70 (d, J=11.2 Hz, 1H), 1.60-1.40 (m, 3H), 1.22 (d,
J=18.0 Hz, 9H), 1.07 (d, J=6.4 Hz, 3H), 0.93 (d, J=6.4 Hz, 3H).
[0288] NaOH (5.5 g, 138.0 mmol, 1.5 eq) was added to a solution of
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-5-(methoxymethoxy)-4,7,9,12-tetram-
ethyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulene-7-carbaldehyde
(35.0 g, 92.0 mmol, 1.0 eq) in MeOH (100 mL). The mixture was
stirred at 20.degree. C. for 0.5 hour. The solvent was evaporated
and 200 mL water was added to the mixture, adjusted pH=6-7 with 2N
HCl. The mixture was treated with DCM (100 mL.times.2). The
combined organic phase was dried over Na.sub.2SO.sub.4 and
concentrated in vacuo to give
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-5-(methoxymethoxy)-4,7,9,12-tetram-
ethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one (32.0 g,
crude) as yellow solid. .sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta.
4.79-4.67 (m, 2H), 4.31 (d, J=9.2 Hz, 1H), 3.54-3.45 (m, 1H), 3.42
(s, 3H), 3.22-3.19 (m, 3H), 2.93 (d, J=6.4 Hz, 1H), 2.64 (m, 1H),
2.32-2.14 (m, 2H), 2.04-1.93 (m, 3H), 1.69 (d, J=11.0 Hz, 1H),
1.62-1.42 (m, 3H), 1.38-1.09 (m, 6H), 1.07 (d, J=6.0 Hz, 3H), 0.98
(m, 6H).
[0289] NaH (2.8 g, 56.7 mmol, 60%, 4.0 eq) was added to a solution
of
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-5-(methoxymethoxy)-4,7,9,12-tetram-
ethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one (5.0 g,
14.2 mmol, 1.0 eq) in THE (20 mL) at 50.degree. C., half an hour
later, allyl bromide (8.9 g, 70.9 mmol, 5.0 eq) was added to the
mixture. The mixture was stirred at 50.degree. C. for 12 hours. The
reaction was quenched by addition of 50 ml water and was treated
with EtOAc(30 mL.times.3). The combined organic phase was dried
over Na.sub.2SO.sub.4 and concentrated in vacuo to give
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-allyl-3-methoxy-5-(methoxymethoxy)-4,7,9,1-
2-tetramethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one
(5.3 g, crude) as yellow oil. .sup.1H NMR (CDCl.sub.3, 400 MHz)
.delta. 5.58 (m, 1H), 5.14-5.01 (m, 2H), 4.77-4.66 (s, 2H), 4.38
(d, J=9.6 Hz, 1H), 3.54-3.34 (s, 3H), 3.29-3.14 (s, 3H), 3.05 (d,
J=6.4 Hz, 1H), 2.75 (dd, J=7.2, 14.0 Hz, 1H), 2.44-2.13 (m, 3H),
2.07-1.88 (m, 1H), 1.82 (d, J=16.0 Hz, 1H), 1.70-1.44 (m, 5H),
1.36-1.10 (m, 10H), 1.07 (s, 3H), 0.98 (dd, J=6.4, 12.4 Hz,
3H).
[0290]
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-allyl-3-methoxy-5-(methoxymethoxy)-4-
,7,9,12-tetramethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one
(5.3 g, 13.5 mmol, 1.0 eq) in HCl (2 M, 6.7 mL, 1.0 eq) and MeOH
(25 mL) were stirred at 15.degree. C. for 12 hours. The mixture was
treated with DCM (50 mL) and water 100 mL, and the aqueous phase
was treated with DCM (50 mL.times.2). The combined organic phase
was dried over Na.sub.2SO.sub.4 and concentrated in vacuo to give
crude product which was purified by flash column(petroleum
ether/EtOAc=20/1-5/1) to give
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-allyl-5-hydroxy-3-methoxy-4,7,9,12-tetrame-
thyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one (3.4 g,
9.8 mmol, 72.3% yield) as white solid. .sup.1H NMR (CDCl.sub.3, 400
MHz) .delta. 5.73-5.60 (m, 1H), 5.18-5.08 (m, 2H), 4.64 (dd, J=6.0,
9.6 Hz, 1H), 3.46 (m, 1H), 3.27-3.17 (m, 3H), 3.13-3.01 (m, 1H),
2.60-2.48 (m, 1H), 2.46-2.29 (m, 2H), 2.26-2.13 (m, 1H), 2.08-1.88
(m, 2H), 1.76-1.55 (m, 4H), 1.54-1.17 (m, 5H), 1.17-1.03 (m, 9H),
0.97 (d, J=6.5 Hz, 3H).
[0291]
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-allyl-5-hydroxy-3-methoxy-4,7,9,12-t-
etramethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one (3.4
g, 9.8 mmol, 1.0 eq), perfluorophenyl 2-(tosyloxy)acetate (7.7 g,
19.5 mmol, 2.0 eq) and DMAP (1.2 g, 9.8 mmol, 1.0 eq) in THE (15.00
mL) were stirred at 20.degree. C. for 12 hours. The solvent was
concentrated in vacuo directly and the crude product was purified
by flash column chromatography (Petroleum ether/EtOAc=1/0-5/1) to
give
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-allyl-3-methoxy-4,7,9,12-tetramethyl-8-oxo-
decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)acetate
(4.5 g, crude) as yellow oil. .sup.1H NMR (CDCl.sub.3, 400 MHz)
.delta. 7.88-7.81 (m, 2H), 7.41-7.35 (m, 2H), 5.89 (d, J=9.6 Hz,
1H), 5.57-5.43 (m, 1H), 5.15-4.99 (m, 3H), 4.65 (dd, J=6.0, 10.0
Hz, 1H), 4.54 (s, 2H), 3.42 (m, 1H), 3.29-3.16 (m, 4H), 3.14-3.03
(m, 2H), 2.81 (dd, J=7.2, 14.8 Hz, 1H), 2.47 (s, 3H), 2.39 (dd,
J=10.0, 15.2 Hz, 2H), 2.28-2.15 (m, 3H), 2.07-1.88 (m, 3H),
1.75-1.41 (m, 7H), 1.38-0.94 (m, 3H), 0.74 (d, J=6.4 Hz, 3H).
[0292] 7-fluoro-1-hydroxy-3H-2,1-benzoxaborol-6-ol (179.7 mg, 1.1
mmol, 1.0 eq),
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-allyl-3-methoxy-4,7,9,12-tetramet-
hyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)acetat-
e (600 mg, 1.1 mmol, 1.0 eq) and Na.sub.2CO.sub.3 (340.2 mg, 3.2
mmol, 3.0 eq) in DMSO (20 mL) were stirred at 30-40.degree. C. for
12 hours. The reaction was quenched by addition of 50 mL water and
adjusted pH<4 with 2N HCl aqueous solution. White solid was
precipitated and filtered to give crude product
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-allyl-3-methoxy-4,7,9,12-tetramethyl-8-oxo-
decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3--
dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (590.0 mg, crude) as
brown solid.
[0293] ZnCl.sub.2 saturated in Con. HCl (1.1 mmol, 10.0 mL, 1.0 eq)
was added to a mixture of
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-allyl-3-methoxy-4,7,9,12-tetramethyl-8-oxo-
decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3--
dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (600.0 mg, 1.1 mmol,
1.0 eq) in THE (20 mL) at 15.degree. C., the mixture was stirred at
15.degree. C. for 2 hours. The mixture was treated with DCM 50 mL
and water 50 mL, the aqueous phase was treated with DCM 20
mL.times.2. The combined organic phase was dried over
Na.sub.2SO.sub.4 and concentrated in vacuo. The crude product was
purified by prep-HPLC (column: Luna C18 100.times.30 mm, 5 .mu.m;
liquid phase: [A-TFA/H.sub.2O=0.075% v/v; B-ACN, B %: 43%-73%, 12
min]). The mixture was concentrated to about 20 mL solution left
and lyophilized to give
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-allyl-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-
decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3--
dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (133.0 mg, 243.9
umol, 22.6% yield, 99.5% purity) as white solid. .sup.1H NMR
(DMSO-d.sub.6, 400 MHz) .delta. 9.19 (s, 1H), 7.24 (t, J=8.0 Hz,
1H), 7.11 (d, J=8.0 Hz, 1H), 5.68 (d, J=8.4 Hz, 1H), 5.66-5.56 (m,
1H), 4.99-4.70 (m, 6H), 3.37 (d, J=5.6 Hz, 1H), 2.37 (br. s., 1H),
2.27-2.00 (m, 5H), 1.83 (dd, J=8.0, 15.6 Hz, 1H), 1.73-1.57 (m,
2H), 1.54-0.96 (m, 10H), 0.90-0.74 (m, 5H), 0.64 (d, J=6.4 Hz,
3H).MS (ESI): mass calcd. For C.sub.30H.sub.40BFO.sub.7 542.44, m/z
found 541.3[M-H].sup.-. HPLC: 99.5% (220 nm), 90.7% (254 nm).
[0294] 22.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-7-(prop-
-2-yn-1-yl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-h-
ydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00130##
[0295] To a solution of
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-5-(methoxymethoxy)-4,7,9,12-tetram-
ethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one (1.5 g,
4.3 mmol, 1.0 eq.) and 3-bromoprop-1-yne (3.8 g, 25.6 mmol, 2.75
mL, 6.0 eq.) in THE (50 mL) was added NaH (1.2 g, 29.8 mmol, 60%
purity, 7.0 eq.). The mixture was stirred at 50.degree. C. for 16
hours. TLC indicated the starting material was consumed. The
reaction mixture was quenched by addition H.sub.2O 50 mL, and then
diluted with EtOAc 50 mL and extracted with EtOAc 150 mL (50
mL.times.3). The combined organic layers were washed with brine 100
mL, dried over Na.sub.2SO.sub.4, filtered and concentrated under
reduced pressure to give a residue. The residue was purified by
column chromatography (SiO.sub.2, petroleum ether/ethyl
acetate=20/1 to 10:1).
(3R,3aS,4R,5R,7R,9R,9aR,12R)-3-methoxy-5-(methoxymethoxy)-4,7,9,12-tetram-
ethyl-7-(prop-2-yn-1-yl)octahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-o-
ne (1.5 g, 3.8 mmol, 90.2% yield) was obtained as colorless.
[0296] To a solution of
(3R,3aS,4R,5R,7R,9R,9aR,12R)-3-methoxy-5-(methoxymethoxy)-4,7,9,12-tetram-
ethyl-7-(prop-2-yn-1-yl)octahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-o-
ne (1.5 g, 3.8 mmol, 1.0 eq.) in THE (70 mL) and CH.sub.3OH (20 mL)
was added HCl (4M, 10.0 mL). The mixture was stirred at 25.degree.
C. for 24 hrs. TLC indicated the starting material was consumed
completely. The reaction mixture was quenched by addition H.sub.2O
60 mL, and then extracted with DCM 150 mL (50 mL.times.3). The
combined organic layers were washed with brine 100 mL, dried over
Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure
to give a residue. The residue was purified by column
chromatography (SiO.sub.2, petroleum ether/ethyl acetate=20/1 to
5:1).
(3R,3aS,4R,5R,7R,9R,9aR,12R)-5-hydroxy-3-methoxy-4,7,9,12-tetramethyl-7-(-
prop-2-yn-1-yl)octahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one
(1.1 g, 3.0 mmol, 78.9% yield) was obtained as a white solid.
.sup.1H NMR (CDCl.sub.3, 400 MHz) .delta. 4.58 (dd, J=5.6, 9.6 Hz,
1H), 3.49-3.41 (m, 1H), 3.22 (s, 3H), 3.02 (q, J=6.0 Hz, 1H),
2.76-2.67 (m, 1H), 2.51 (dd, J=2.4, 17.2 Hz, 1H), 2.42 (dd, J=9.6,
15.6 Hz, 1H), 2.26-2.17 (m, 1H), 2.09 (br. s., 1H), 2.06-1.94 (m,
2H), 1.74 (d, J=4.0 Hz, 1H), 1.71 (s, 1H), 1.57 (s, 4H), 1.51 (d,
J=5.7 Hz, 2H), 1.38-1.31 (m, 1H), 1.26-1.19 (m, 3H), 1.17-1.11 (m,
3H), 1.08 (d, J=7.2 Hz, 3H), 1.02 (d, J=6.0 Hz, 3H).
[0297] To a solution of
(3R,3aS,4R,5R,7R,9R,9aR,12R)-5-hydroxy-3-methoxy-4,7,9,12-tetramethyl-7-(-
prop-2-yn-1-yl)octahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one
(1.1 g, 3.0 mmol, 1.0 eq.) and perfluorophenyl 2-(tosyloxy)acetate
(2, 3, 4, 5, 6-pentafluoro-phenyl) 2-(p-tolylsulfonyloxy) acetate
(1.8 g, 4.6 mmol, 1.5 eq.) in THE (50 mL) was added DMAP (370.1 mg,
3.0 mmol, 1.0 eq.). The mixture was stirred at 25.degree. C. for 16
hours. TLC indicated the starting material was consumed completely.
The reaction mixture was concentrated under reduced pressure to
remove THE to give a residue. The residue was purified by column
chromatography (SiO.sub.2, petroleum ether/ethyl acetate=20/1 to
7:1) to give
(3R,3aS,4R,5R,7R,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-8-oxo-7-(prop-
-2-yn-1-yl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)acet-
ate (1.5 g, 2.7 mmol, 88.6% yield) as a white solid. .sup.1H NMR
(CDCl.sub.3, 400 MHz) .delta. 7.85 (d, J=7.6 Hz, 2H), 7.38 (d,
J=8.0 Hz, 2H), 5.77 (d, J=10.0 Hz, 1H), 4.54 (s, 2H), 3.45-3.37 (m,
1H), 3.22 (s, 3H), 3.12-3.01 (m, 2H), 2.50-2.37 (m, 1H), 2.33-2.21
(m, 2H), 2.06-1.95 (m, 3H), 1.71 (d, J=11.0 Hz, 1H), 1.60-1.45 (m,
2H), 1.30 (d, J=16.4 Hz, 2H), 1.22-1.12 (m, 8H), 1.10-1.03 (m, 4H),
0.87 (d, J=6.8 Hz, 3H), 0.73 (d, J=6.8 Hz, 3H).
[0298] To a solution of
(3R,3aS,4R,5R,7R,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-8-oxo-7-(prop-
-2-yn-1-yl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)acet-
ate (800.0 mg, 1.4 mmol, 1.0 eq.) and 7-fluoro-1-hydroxy-3H-2,
1-benzoxaborol-6-ol (240.1 mg, 1.4 mmol, 1.0 eq.) in DMSO (10 mL)
was added Na.sub.2CO.sub.3 (151.6 mg, 1.4 mmol, 1.0 eq.). The
mixture was stirred at 40.degree. C. for 16 hours. HPLC indicated
the starting material was consumed completely. The reaction mixture
was quenched by addition H.sub.2O 50 mL, and then adjusted pH=7,
filtered to give crude product to give
(3R,3aS,4R,5R,7R,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-8-oxo-7-(prop-
-2-yn-1-yl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-h-
ydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (900.0 mg,
crude) as light gray solid, which was used into the next step
without further purification.
[0299] To a solution of
(3R,3aS,4R,5R,7R,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-8-oxo-7-(prop-
-2-yn-1-yl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-h-
ydroxyl-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (500.0
mg, 901.8 umol, 1.0 eq.) in THE (20 mL) was added ZnCl.sub.2/HCl
(901.8 umol, 15.0 mL). The mixture was stirred at 25.degree. C. for
2 hours. HPLC indicated the starting material was consumed
completely. The reaction mixture was quenched by addition H.sub.2O
50 mL, and then extracted with DCM 150 mL (50 mL.times.3). The
combined organic layers were washed with brine 80 mL, dried over
Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure
to give a residue. The residue was purified by prep-HPLC (column:
Waters Xbridge 150.times.25 mm, 5 .mu.m; liquid phase: [A-10 mM
NH.sub.4HCO.sub.3 in H.sub.2O; B-ACN, B %: 20%-50%, 12 min)
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-7-(prop-
-2-yn-1-yl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-h-
ydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (170.0 mg,
314.6 umol, 34.9% yield) as a white solid. .sup.1H NMR
(DMSO-d.sub.6, 400 MHz) .delta. 9.26 (s, 1H), 7.23 (t, J=8.0 Hz,
1H), 7.12 (s, 1H), 5.65 (d, J=7.6 Hz, 1H), 4.93 (s, 2H), 4.85-4.64
(m, 4H), 3.43 (br. s., 1H), 2.63 (br. s., 1H), 2.41-2.25 (m, 3H),
2.23-2.01 (m, 4H), 1.88 (dd, J=7.6, 15.6 Hz, 1H), 1.73-1.56 (m,
3H), 1.54-1.39 (m, 3H), 1.34-1.20 (m, 2H), 1.07-0.97 (m, 4H),
0.88-0.74 (m, 3H), 0.63 (d, J=6.0 Hz, 3H). MS (ESI): mass calcd.
for C.sub.30H.sub.38BFO.sub.7 540.43, m/z found 539.4 [M-H].sup.-.
HPLC: 96.49% (220 nm), 84.56% (254 nm). [0300] 23.
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-7-(hydroxymethyl)-4,7,9,12-tetrame-
thyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hy-
droxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00131##
[0301]
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-formyl-8-hydroxy-4,7,9,12-tetramethy-
l-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)acetate
(300.0 mg, 561.1 umol, 1.0 eq) and NaBH(OAc).sub.3 (237.8 mg, 1.1
mmol, 2.0 eq) in DCM (15.0 mL) were stirred at 20.degree. C. for 2
hours. 20 mL water was added to the mixture, the aqueous layer was
treated with DCM (10 mL.times.3), the combined organic phase was
treated with brine, dried over Na.sub.2SO.sub.4 and concentrated in
vacuo to give crude
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-7-(hydroxymethyl)-4,7,9,12-tetrame-
thyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)aceta-
te (300.0 mg, crude) as colorless oil.
[0302]
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-7-(hydroxymethyl)-4,7,9,12-t-
etramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy-
)acetate (300.0 mg, 559.0 umol, 1.0 eq),
7-fluoro-1-hydroxy-3H-2,1-benzoxaborol-6-ol (93.9 mg, 559.0 umol,
1.0 eq) and Na.sub.2CO.sub.3 (177.7 mg, 1.7 mmol, 3.0 eq) in DMSO
(5.0 mL) were heated to 30-40.degree. C. for 12 hours. 20 mL water
was added to the mixture; white solid was precipitated and filtered
to give crude product. The crude product was purified by prep-HPLC
(column: Luna C18 100.times.30 mm, 5 .mu.m; liquid phase:
[A-TFA/H.sub.2O=0.075% v/v; B-ACN]B %: 35%-70%, 12 min]) to give
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-7-(hydroxymethyl)-4,7,9,12-tetrame-
thyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hy-
droxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (47.0 mg,
88.3 umol, 15.8% yield) as white solid. .sup.1H NMR (DMSO-d.sub.6,
400 MHz) .delta. 9.26 (s, 1H), 7.22-7.20 (m, 1H), 7.10-7.00 (m,
1H), 5.55-5.53 (m, 1H), 5.17-5.15 (m, 1H), 4.92 (s, 1H), 4.83-4.72
(m, 3H), 4.56-4.48 (m, 2H), 3.90 (d, J=11.0 Hz, 1H), 3.41 (d, J=6.2
Hz, 1H), 3.32 (d, J=11.0 Hz, 1H), 2.32-2.30 (m, 2H), 2.26-1.98 (m,
3H), 1.88-1.21 (m, 10H), 1.02 (s, 3H), 0.83 (d, J=7.1 Hz, 3H), 0.61
(d, J=6.6 Hz, 3H). MS (ESI): mass calcd. for
C.sub.28H.sub.38BFO.sub.8 532.3, m/z found 531.3 [M-H].sup.-. HPLC:
100% in 220 nm; 100% in 254 nm. [0303] 24.
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-7-(methoxymethyl)-4,7,9,12-tetrame-
thyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hy-
droxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00132##
[0304] To a solution of
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-5-(methoxymethoxy)-4,7,9,12-tetram-
ethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one (3.0 g,
8.5 mmol, 1.0 eq) in THE (20 mL) was added KHMDS (1M, 51.1 mL, 6.0
eq) at -78.degree. C. over 30 mins, followed by MOMCl (3.4 g, 42.6
mmol, 3.2 mL, 5.0 eq). The mixture was stirred at 25.degree. C. for
15 hrs. The reaction mixture was quenched by addition water 50 mL
at 0.degree. C., and then diluted with EtOAc 20 mL and extracted
with EtOAc (50 mL.times.2). The combined organic layers were washed
with brine (100 mL.times.2), dried over Na.sub.2SO.sub.4, filtered
and concentrated under reduced pressure to give a residue. The
residue was purified by column chromatography (SiO.sub.2, petroleum
ether/ethyl acetate=50/1 to 30:1) to afford
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-5-(methoxymethoxy)-7-(metho-
xymethyl)-4,7,9,12-tetramethyloctahydro-4,9a-propanocyclopenta[8]annulen-8-
(9H)-one (2.2 g, 5.6 mmol, 65.2% yield) as colorless oil.
[0305] To a solution of
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-5-(methoxymethoxy)-7-(methoxymethy-
l)-4,7,9,12-tetramethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-on-
e (2.2 g, 5.6 mmol, 1.0 eq) in THE (20 mL) and MeOH (5 mL) was
added HCl (4M, 5 mL, 3.6 eq). The mixture was stirred at 25.degree.
C. for 20 hrs. The reaction mixture was quenched by addition water
50 mL at 20.degree. C., and then diluted with EtOAc 20 mL and
extracted with EtOAc (50 mL.times.2). The combined organic layers
were washed with brine (100 mL.times.2), dried over
Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure
to give a residue. The residue was purified by column
chromatography (SiO.sub.2, petroleum ether/ethyl acetate=30/1 to
10:1) to afford
(3R,3aS,4R,5R,7S,9R,9aR,12R)-5-hydroxy-3-methoxy-7-(methoxymethyl)-
-4,7,9,12-tetramethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one
(1.3 g, 3.7 mmol, 66.5% yield) as a white solid. .sup.1H NMR
(CDCl.sub.3, 400 MHz) .delta. 4.66 (dd, J=5.6, 9.6 Hz, 1H), 3.89
(d, J=9.2 Hz, 1H), 3.49-3.41 (m, 1H), 3.33 (s, 3H), 3.21 (s, 3H),
3.06 (q, J=6.4 Hz, 1H), 2.38-2.19 (m, 2H), 2.07-1.94 (m, 2H), 1.72
(d, J=11.6 Hz, 1H), 1.64-1.45 (m, 5H), 1.40-1.16 (m, 4H), 1.14 (d,
J=8.4 Hz, 7H), 1.08 (d, J=7.2 Hz, 3H), 0.96 (d, J=6.4 Hz, 3H).
[0306] To a solution of
(3R,3aS,4R,5R,7S,9R,9aR,12R)-5-hydroxy-3-methoxy-7-(methoxymethyl)-4,7,9,-
12-tetramethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one
(1.3 g, 3.7 mmol, 1.0 eq) and (2,3,4,5,6-pentafluorophenyl)
2-(p-tolylsulfonyloxy)acetate (2.2 g, 5.6 mmol, 1.5 eq) in THE (20
mL) was added DMAP (450.8 mg, 3.7 mmol, 1.0 eq). The mixture was
stirred at 25.degree. C. for 15 hrs. The solid was filtered and the
filtrate was concentrated to give a residue. The residue was
purified by column chromatography (SiO.sub.2, petroleum ether/ethyl
acetate=30/1 to 10:1) to afford
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-7-(methoxymethyl)-4,7,9,12--
tetramethyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosylox-
y)acetate (1.0 g, 1.8 mmol, 48.0% yield) as a white solid. .sup.1H
NMR (CDCl.sub.3, 400 MHz) .delta. 7.85-7.80 (m, 2H), 7.36 (d, J=8.0
Hz, 2H), 5.78 (d, J=10.0 Hz, 1H), 4.50 (d, J=1.8 Hz, 2H), 4.10 (d,
J=9.6 Hz, 1H), 3.46-3.36 (m, 1H), 3.29 (d, J=2.0 Hz, 3H), 3.19 (s,
3H), 3.10-3.03 (m, 1H), 2.45 (s, 3H), 2.36-2.18 (m, 3H), 2.00 (d,
J=13.2 Hz, 2H), 1.68 (d, J=11.6 Hz, 1H), 1.54-1.38 (m, 3H),
1.35-1.00 (m, 10H), 0.95 (d, J=6.8 Hz, 3H), 0.71 (d, J=7.2 Hz,
3H).
[0307] A mixture of
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-7-(methoxymethyl)-4,7,9,12-tetrame-
thyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)aceta-
te (600.0 mg, 1.1 mmol, 1.0 eq), F-OHCBO (178.0 mg, 1.1 mmol, 1.0
eq), Na.sub.2CO.sub.3 (224.7 mg, 2.1 mmol, 2.0 eq) and KI (88.0 mg,
530.0 umol, 0.5 eq) in DMSO (20 mL) was degassed and purged with
N.sub.2 for 3 times, and then the mixture was stirred at 40.degree.
C. for 4 hrs under N.sub.2 atmosphere. The reaction mixture was
quenched by addition water 50 mL at 0.degree. C., then adjusted pH
to 4-5 by 4N HCl, the solid was precipitated, filtered, the solid
was washed with water for three times, then washed with petroleum
ether for three times to afford
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-7-(methoxymethyl)-4,7,9,12-tetrame-
thyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hy-
droxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (500.0 mg,
892.1 umol, 84.2% yield) as a pink solid.
[0308] To a solution of
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-7-(methoxymethyl)-4,7,9,12-tetrame-
thyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hy-
droxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (500.0 mg,
892.1 umol, 1.0 eq) in THE (20 mL) was added ZnCl.sub.2 in HCl
(213.5 mmol, 10.0 mL, 239.3 eq). The mixture was stirred at
25.degree. C. for 15 hrs. The reaction mixture was quenched by
addition water 20 mL at 0.degree. C., and then diluted with EtOAc
10 mL and extracted with EtOAc (20 mL.times.3). The combined
organic layers were washed with brine (100 mL.times.1), dried over
Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure
to give a residue. The residue was purified by prep-HPLC (column:
Luna C18 100.times.30 mm, 5 .mu.m; liquid phase:
[A-TFA/H.sub.2O=0.075% v/v; B-ACN, B %: 35%-75%, 12 min, MeCN was
removed under reduced pressure, the residue was dried under
freeze-drying to afford
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-7-(methoxymethyl)-4,7,9,12--
tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluo-
ro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(235.0 mg, 430.1 umol, 48.2% yield) as a white solid. .sup.1H NMR
(DMSO-d.sub.6, 400 MHz) .delta. 7.20 (t, J=8.0 Hz, 1H), 7.10 (d,
J=8.4 Hz, 1H), 5.65 (d, J=8.4 Hz, 1H), 4.91 (s, 2H), 4.83-4.71 (m,
2H), 3.47-3.33 (m, 3H), 3.08 (s, 3H), 2.35 (br. s., 1H), 2.24-1.99
(m, 4H), 1.79-1.22 (m, 13H), 0.98 (s, 3H), 0.80 (d, J=7.2 Hz, 3H),
0.63 (d, J=7.2 Hz, 3H). MS (ESI): mass calcd. for
C.sub.29H.sub.40BFO.sub.8 546.43, m/z found 545.3 [M-1].sup.-.
HPLC: 99.7% (220 nm), 97.5% (254 nm). [0309] 25.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-7-(2-hydroxyethyl)-4,7,9,12-tetram-
ethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-h-
ydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00133##
[0310] NaBH(OAc).sub.3 (453.6 mg, 2.1 mmol, 2.0 eq) was added to a
solution of
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-8-oxo-7-(2-ox-
oethyl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)acetate
(600.0 mg, 1.1 mmol, 1.0 eq) in DCM (20 mL) at 20.degree. C. The
mixture was stirred at this temperature for 12 hours. LCMS showed
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-8-oxo-7-(2-ox-
oethyl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)acetate
consumed, one major peak was detected. The reaction was quenched by
addition of 50 mL water, and treated with DCM (50 mL.times.3). The
combined organic phase was dried over Na.sub.2SO.sub.4 and
concentrated in vacuo to give
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-(2-hydroxyethyl)-3-methoxy-4,7,9,12-tetram-
ethyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)acet-
ate (600.0 mg, crude) as brown solid. MS (ESI): mass calcd. for
C.sub.30H.sub.44O.sub.8S 564.28, m/z found 563[M-H].sup.-.
[0311] 7-fluoro-1-hydroxy-3H-2,1-benzoxaborol-6-ol (178.4 mg, 1.1
mmol, 1.0 eq),
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-(2-hydroxyethyl)-3-methoxy-4,7,9,-
12-tetramethyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosy-
loxy)acetate (600.0 mg, 1.1 mmol, 1.0 eq) and Na.sub.2CO.sub.3
(337.8 mg, 3.2 mmol, 3.0 eq) in DMSO (20 mL) were stirred at
30-40.degree. C. for 12 hours. The reaction was quenched by
addition of 50 mL water, and adjusted by addition of 2N HCl till
pH<4, white solid was precipitated and filtered to give
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-(2-hydroxyethyl)-3-methoxy-4,7,9,12-tetram-
ethyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-h-
ydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (600.00
mg, crude) as brown solid.
[0312] ZnCl.sub.2 saturated in Con.HCl (1.1 mmol, 10.0 mL) was
added to a solution of
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-(2-hydroxyethyl)-3-methoxy-4,7,9,12-tetram-
ethyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-h-
ydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (600.0 mg,
1.1 mmol, 1.0 eq) in THE (20 mL) at 20.degree. C. The mixture was
stirred at 20.degree. C. for 6 hours. LCMS showed
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-(2-hydroxyethyl)-3-methoxy-4,7,9,12-tetram-
ethyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-h-
ydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate consumed,
one new peak MS=527 (M-H).sup.-. The mixture was treated with DCM
50 mL and 50 ml water, the aqueous phase was treated with DCM (30
mL.times.3). The combined organic phase was treated with
Na.sub.2SO.sub.4 and concentrated in vacuo to give crude product.
The crude product was purified by prep-HPLC (column: Luna C8
100.times.30 mm, 5 .mu.m; liquid phase: [A-TFA/H.sub.2O=0.075% v/v;
B-ACN, B %: 50%-70%, 12 min]). The mixture was concentrated to 20
mL solution left and lyophilized to give
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-7-(2-hydroxyethyl)-4,7,9,12-tetram-
ethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-h-
ydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (68.0 mg,
128.7 umol, 12.0% yield) as white solid. .sup.1H NMR (DMSO-d.sub.6,
400 MHz) .delta. 9.27 (s, 1H), 7.27-7.21 (m, 1H), 7.10 (d, J=8.0
Hz, 1H), 5.71 (d, J=9.2 Hz, 1H), 5.18-5.06 (m, 2H), 4.92 (s, 2H),
4.87 (d, J=2.8 Hz, 2H), 3.67-3.63 (m, 3H), 2.41 (s, 1H), 2.25-1.88
(m, 5H), 1.66-1.62 (m, 2H), 1.42-1.29 (m, 8H), 1.03-1.00 (m, 4H),
0.81 (d, J=6.4 Hz, 3H), 0.67 (d, J=7.2 Hz, 3H). MS (ESI): mass
calcd. for C.sub.29H.sub.40BFO.sub.8 546.28, m/z found
527[M-H.sub.2O-H].sup.-. HPLC: 99.6% (220 nm), 100% (254 nm).
[0313] 26.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-7-(2-methoxyethyl)-4,7,9,12-tetram-
ethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-h-
ydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00134##
[0314] To a solution of
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-5-(methoxymethoxy)-4,7,9,12-tetram-
ethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one (2.0 g,
5.7 mmol, 1.0 eq) in THE (30.0 mL) was added KHMDS (1 M, 34.0 mL,
6.0 eq) at -78.degree. C. The mixture was stirred at -78.degree. C.
for 1 hour. Then 1-bromo-2-methoxy-ethane (3.9 g, 28.4 mmol, 2.7
mL, 5.0 eq) was added the mixture and stirred at 25.degree. C. for
12 hours. TLC (petroleum ether/ethyl acetate=10/1, RF 0.35) showed
the reaction was complete. H.sub.2O (60 mL) was added to the
mixture. The mixture was extracted with ethyl acetate (40
mL.times.3). The combined organic phase was washed with brine (20
mL), dried with anhydrous Na.sub.2SO.sub.4, filtered and
concentrated in vacuum to give crude product, which was purified by
silica gel chromatography (Petroleum ether) to afford
(3R,3aS,4R,5R,7R,9R,9aR,12R)-3-methoxy-7-(2-methoxyethyl)-5-(methoxymetho-
xy)-4,7,9,12-tetramethyloctahydro-4,9a-propanocyclopenta
[8]annulen-8(9H)-one (2.0 g, 4.9 mmol, 85.9% yield) as colorless
oil.
[0315] To a mixture of
(3R,3aS,4R,5R,7R,9R,9aR,12R)-3-methoxy-7-(2-methoxyethyl)-5-(methoxymetho-
xy)-4,7,9,12-tetramethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-o-
ne (2.0 g, 4.9 mmol, 1.0 eq) in MeOH (10.0 mL) was added HCl (2 M,
10.0 mL, 4.1 eq) in one portion at 25.degree. C. The mixture was
stirred at 25.degree. C. for 12 hours. TLC (petroleum ether/ethyl
acetate=10/1, RF 0.3) showed the reaction was complete. H.sub.2O
(50 mL) was added the mixture, which was extracted with EtOAc (50
mL.times.3). The combined organic layers were washed with brine (30
mL) and dried over Na.sub.2SO.sub.4. After filtration via filter
paper, the organic layer was concentrated under reduced pressure to
provide crude product, which was purified by silica gel
chromatography (petroleum ether/ethyl acetate=50/1) to afford
product
(3R,3aS,4R,5R,7R,9R,9aR,12R)-5-hydroxy-3-methoxy-7-(2-methoxyethyl)-4,7,9-
,12-tetramethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one
(1.3 g, 3.6 mmol, 72.9% yield) as light yellow oil. .sup.1H NMR
(CDCl.sub.3, 400 MHz) .delta. 4.62 (d, J=8.8 Hz, 1H), 3.57-3.40 (m,
2H), 3.33 (s, 3H), 3.21 (s, 3H), 3.16 (d, J=6.4 Hz, 1H), 2.38 (m,
1H), 2.24-1.91 (m, 4H), 1.89-1.45 (m, 8H), 1.19 (s, 3H), 1.14 (m,
3H), 1.11-1.04 (m, 6H), 0.98 (d, J=6.4 Hz, 3H).
[0316] To a solution of
(3R,3aS,4R,5R,7R,9R,9aR,12R)-5-hydroxy-3-methoxy-7-(2-methoxyethyl)-4,7,9-
,12-tetramethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one
(1.3 g, 3.5 mmol, 1.0 eq) and compound perfluorophenyl
2-(tosyloxy)acetate (1.8 g, 4.5 mmol, 1.3 eq) in THE (25.0 mL) was
added DMAP (853.7 mg, 7.0 mmol, 2.0 eq) at 25.degree. C. The
mixture was stirred at 25.degree. C. for 18 hours. H.sub.2O (30 mL)
was added the mixture. The aqueous layer was extracted with EtOAc
(20 mL.times.3). The combined organic layers were washed with brine
(10 mL) and dried over Na.sub.2SO.sub.4. After filtration via
filter paper, the organic layer was concentrated under reduced
pressure to provide crude product, which was purified by silica gel
chromatography (petroleum ether/ethyl acetate=100/1, 20/1, 10/1) to
afford product
(3R,3aS,4R,5R,7R,9R,9aR,12R)-3-methoxy-7-(2-methoxyethyl)-4,7,9,12-tetram-
ethyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl-2-(tosyloxy)ace-
tate (560.0 mg, 967.6 umol, 27.7% yield) as light yellow solid.
.sup.1H NMR (CDCl.sub.3, 400 MHz) .delta. 7.85 (d, J=7.9 Hz, 2H),
7.37 (d, J=7.9 Hz, 2H), 5.84 (d, J=10.1 Hz, 1H), 4.62 (d, J=9.3 Hz,
2H), 4.53 (s, 2H), 3.56-3.38 (m, 4H), 3.26 (s, 3H), 3.18-3.09 (m,
4H), 2.47 (s, 3H), 2.44-2.27 (m, 4H), 1.89-1.76 (m, 4H), 1.70 (d,
J=11.6 Hz, 4H), 1.31-1.25 (m, 5H), 0.93-0.78 (m, 3H), 0.73 (d,
J=6.6 Hz, 3H).
[0317] To a solution of compound
7-fluorobenzo[c][1,2]oxaborole-1,6(3H)-diol (145.0 mg, 863.5 umol,
1.0 eq) and
(3R,3aS,4R,5R,7R,9R,9aR,12R)-3-methoxy-7-(2-methoxyethyl)-4,7,9,1-
2-tetramethyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyl-
oxy)acetate (549.7 mg, 949.8 umol, 1.1 eq) in DMSO (10.0 mL) was
added Na.sub.2CO.sub.3 (274.6 mg, 2.6 mmol, 3.0 eq) and KI (143.3
mg, 863.5 umol, 1.0 eq) at 25.degree. C. under N.sub.2. The
reaction mixture was stirred at 25.degree. C. for 5 hours. H.sub.2O
(80 mL) was added the mixture, which was acidified with aqueous HCl
(2 M) till pH=5-6 to precipitate a white solid. The reaction
mixture was filtered and the filter cake was washed with H.sub.2O
(20 mL.times.4) to give a white solid, which was dissolved in DCM
(20 mL) and dried over Na.sub.2SO.sub.4. After filtration via
filter paper, the organic layer was concentrated under reduced
pressure to provide product
(3R,3aS,4R,5R,7R,9R,9aR,12R)-3-methoxy-7-(2-methoxyethyl)-4,7,9,12-tetram-
ethyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-h-
ydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (450.0 mg,
crude) as light yellow solid. The crude product was used directly
in the next step.
[0318] To a mixture of
(3R,3aS,4R,5R,7R,9R,9aR,12R)-3-methoxy-7-(2-methoxyethyl)-4,7,9,12-tetram-
ethyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-h-
ydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (450.0 mg,
783.3 umol, 1.0 eq) in THE (5.0 mL) was added ZnCl.sub.2 (10.0 mL
saturated in con.HCl) in one portion at 25.degree. C. The mixture
was stirred at 25.degree. C. for 15 hours. HPLC and LCMS showed the
reaction was complete. The mixture was added H.sub.2O (20 mL). The
aqueous phase was extracted with DCM (20 mL.times.3). The combined
organic phase was washed with brine (10 mL.times.2), dried with
anhydrous Na.sub.2SO.sub.4, filtered and concentrated in vacuum to
give crude product, which was purified by prep-HPLC (column: Luna
C18 100.times.30 mm, 5 .mu.m; liquid phase: [A-TFA/H.sub.2O=0.075%
v/v; B-ACN]B %: 38%-68%, 12 min]). After prep-HPLC purification,
the eluent was concentrated to remove organic solvent. The residual
aqueous solution was lyophilized to give product
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-7-(2-methoxyethyl)-4,7,9,12-tetram-
ethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-h-
ydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (48.0 mg,
84.8 umol, 10.8% yield, 99.0% purity) as white solid. .sup.1H NMR
(DMSO-d.sub.6 400 MHz) .delta. 9.28 (s, 1H), 7.29-7.21 (m, 1H),
7.12 (d, J=8.0 Hz, 1H), 5.60 (d, J=8.0 Hz, 1H), 4.93 (s, 2H), 4.81
(d, J=4.2 Hz, 2H), 4.51 (d, J=6.4 Hz, 1H), 3.29 (m, 2H), 3.19 (d,
J=6.0 Hz, 1H), 3.12 (s, 3H), 2.40-2.36 (m, 1H), 2.00 (s, 3H),
1.71-1.39 (m, 6H), 1.21-1.10 (m, 3H), 1.07-0.97 (m, 5H), 0.92 (s,
3H), 0.82 (d, J=6.4 Hz, 3H), 0.64 (d, J=6.4 Hz, 3H). MS (ESI): mass
calcd. for C.sub.30H.sub.42BFO.sub.8 560.30, m/z found 559.3
[M-H].sup.-. HPLC: 99.0% (220 nm), 88.9% (254 nm). [0319] 27.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-((R)-oxiran-
-2-yl)-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1--
hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate [0320]
28.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-7-((R)-1-hydroxy-2-(methylamino)et-
hyl)-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen--
5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)aceta-
te
##STR00135##
[0321] A mixture of
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-7-vinyl-
decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)acetate
(20.0 g, 37.5 mmol, 1.0 eq), m-CPBA (8.9 g, 41.3 mmol, 1.1 eq) in
DCM (200.0 mL) was degassed and purged with N.sub.2 for 3 times,
and then the mixture was stirred at 25.degree. C. for 12 hours
under N.sub.2 atmosphere. The mixture was poured into ice-water
(w/w=1/1) (100 mL). The combined organic phase was washed with
aq.NaHCO.sub.3(20 mL) and brine (100 mL), dried with anhydrous
Na.sub.2SO.sub.4, filtered and concentrated in vacuum. The residue
was purified by silica gel chromatography (petroleum ether/Ethyl
acetate=1/1) to give
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-((R)-oxiran-
-2-yl)-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)ace-
tate (11.0 g, 20.0 mmol, 53.4% yield) as a white solid.
[0322] A mixture of
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-((R)-oxiran-
-2-yl)-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)ace-
tate (2.0 g, 3.6 mmol, 1.0 eq.),
7-fluoro-1-hydroxy-3H-2,1-benzoxaborol-6-ol (612.9 mg, 3.6 mmol,
1.0 eq.), Na.sub.2CO.sub.3 (1.2 g, 10.9 mmol, 3.0 eq.) in DMSO
(30.0 mL) was degassed and purged with N.sub.2 for 3 times, and
then the mixture was stirred at 30.degree. C. for 12 hours under
N.sub.2 atmosphere. The mixture was poured into ice-water (w/w=1/1)
(50 mL) and precipitating solid. The solid was collected to afford
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-((R)-oxiran-
-2-yl)-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1--
hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (1.7 g,
crude) as a white solid. .sup.1H NMR (DMSO-d.sub.6, 400 MHz)
.delta. 9.27 (s, 1H), 7.25-7.19 (m, 1H), 7.13 (d, J=8.4 Hz, 1H),
5.6 (d, J=8.4 Hz, 1H), 4.97-4.90 (m, 2H), 4.89-4.75 (m, 2H), 4.35
(d, J=6.4 Hz, 1H), 3.48 (t, J=6.4 Hz, 1H), 3.13-3.10 (m, 1H),
2.43-2.37 (m, 1H), 2.30-1.99 (m, 5H), 1.76-1.57 (m, 3H), 1.55-1.23
(m, 6H), 1.18-0.97 (m, 3H), 0.93-0.75 (m, 6H), 0.64 (d, J=7.2 Hz,
3H) MS (ESI): mass calcd. for C.sub.29H.sub.38BFO.sub.8 544.26, m/z
found 543.3 [M-H].sup.-. HPLC: 96.6% (220 nm), 100.0% (254 nm).
[0323] A mixture of
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-((R)-oxiran-
-2-yl)-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1--
hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (500.0
mg, 918.4 umol, 1.0 eq.), methanamine (950.8 mg, 9.2 mmol, 10.0
eq.) in MeOH (20.0 mL) was degassed and purged with N.sub.2 for 3
times, and then the mixture was stirred at 40.degree. C. for 12
hours under N.sub.2 atmosphere. The solvent was concentrated under
reduced pressure at 30.degree. C. to give a residue, which was
purified by prep-HPLC (column: Luna 250.times.50.0 mm, 10 .mu.m;
liquid phase: [A-H.sub.2O+0.075% TFA; B-ACN]B %: 15%-45%, 20 min])
to give
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-7-((R)-1-hydroxy-2-(methylamino)et-
hyl)-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen--
5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)aceta-
te (323.0 mg, 561.2 umol, 61.1% yield) as a white solid. .sup.1H
NMR (DMSO-d.sub.6, 400 MHz) .delta. 7.25 (br. s., 1H), 7.12 (d,
J=8.0 Hz, 1H), 5.44 (d, J=8.0 Hz, 1H), 4.94-4.80 (m, 4H), 4.52 (d,
J=9.8 Hz, 1H), 3.60 (d, J=4.8 Hz, 1H), 2.85-2.76 (m, 1H), 2.68 (d,
J=10.8 Hz, 1H), 2.40-2.30 (m, 4H), 2.27-1.88 (m, 4H), 1.73-1.44 (m,
3H), 1.38-1.13 (m, 7H), 0.99 (s, 4H), 0.89 (d, J=6.4 Hz, 3H), 0.62
(d, J=6.4 Hz, 3H) MS (ESI): mass calcd. for
C.sub.32H.sub.44BF.sub.4NO.sub.10 575.31, m/z found 576.4
[M+H].sup.+. HPLC: 97.1% (220 nm), 93.6% (254 nm). [0324] 29.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-((methylthi-
o)methyl)-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-
-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate [0325]
30.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-((methylsul-
finyl)methyl)-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fl-
uoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00136##
[0326] NaH (852.0 mg, 21.3 mmol, 60% purity, 5.0 eq) was added to a
solution of
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-5-(methoxymethoxy)-4,7,9,12-tetram-
ethyloctahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one (1.5 g,
4.3 mmol, 1.0 eq) in THE (20 mL) at 50.degree. C., half an hour
later chloro(methylsulfanyl)methane (2.5 g, 25.5 mmol, 2.1 mL, 6.0
eq) was added to the mixture and stirred at 50.degree. C. for 12
hours. The reaction was quenched by addition of 100 mL water, and
treated with EtOAc (30 mL.times.3). The combined organic phase was
dried over Na.sub.2SO.sub.4 and concentrated in vacuo. The crude
product was purified by flash column chromatography Petroleum
ether:EtOAc=100:1 to give
(3R,3aS,4R,5R,7R,9R,9aR,12R)-3-methoxy-5-(methoxymethoxy)-4,7,9,12-t-
etramethyl-7-((methylthio)methyl)octahydro-4,9a-propanocyclopenta[8]annule-
n-8(9H)-one (1.5 g, 3.6 mmol, 85.3% yield) as yellow oil. .sup.1H
NMR (DMSO-d.sub.6, 400 MHz) .delta. 4.73 (s, 2H), 4.34 (d, J=9.6
Hz, 1H), 3.50-3.38 (m, 4H), 3.24-3.19 (m, 3H), 3.05-2.96 (m, 2H),
2.80 (d, J=13.2 Hz, 1H), 2.37 (dd, J=9.6, 15.6 Hz, 1H), 2.27-2.18
(m, 1H), 2.17-2.13 (m, 3H), 2.07-1.89 (m, 5H), 1.67 (d, J=11.6 Hz,
1H), 1.54-1.44 (m, 4H), 1.19 (d, J=4.4 Hz, 7H), 1.04 (d, J=6.4 Hz,
3H), 0.99 (d, J=6.5 Hz, 3H).
[0327]
(3R,3aS,4R,5R,7R,9R,9aR,12R)-3-methoxy-5-(methoxymethoxy)-4,7,9,12--
tetramethyl-7-((methylthio)methyl)octahydro-4,9a-propanocyclopenta[8]annul-
en-8(9H)-one (1.9 g, 4.6 mmol, 1.0 eq) and HCl (2 M, 51.3 mL, 22.3
eq) in THE (10 mL) and MeOH (10 mL) were stirred at 20.degree. C.
for 12 hours. The mixture was treated with DCM 50 mL and water 100
mL. The aqueous phase was treated with DCM (50 mL.times.3). The
combined organic phase was dried over Na.sub.2SO.sub.4 and
concentrated in vacuo. The crude product was purified by flash
column chromatography (Petroleum ether/EtOAc=100/1) to give
(3R,3aS,4R,5R,7R,9R,9aR,12R)-5-hydroxy-3-methoxy-4,7,9,12-tetramethyl-7-(-
(methylthio)methyl)octahydro-4,9a-propanocyclo
penta[8]annulen-8(9H)-one (1.2 g, 3.4 mmol, 73.6% yield) as yellow
oil.
[0328] DMAP (412.9 mg, 3.4 mmol, 1.0 eq) was added to a solution of
(3R,3aS,4R,5R,7R,9R,9aR,12R)-5-hydroxy-3-methoxy-4,7,9,12-tetramethyl-7-(-
(methylthio)methyl)octahydro-4,9a-propanocyclopenta[8]annulen-8(9H)-one
(1.2 g, 3.4 mmol, 1.0 eq), perfluorophenyl 2-(tosyloxy)acetate (2.0
g, 5.1 mmol, 1.5 eq) in THE (30 mL). The mixture was stirred at
20.degree. C. for 12 hours. The mixture was purified by flash
column (petroleum ether/EtOAc=10/1) without any work-up to give
(3R,3aS,4R,5R,7R,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-7-((methylthi-
o)methyl)-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)-
acetate (1.5 g, 2.6 mmol, 76.4% yield) as yellow oil. .sup.1H NMR
(DMSO-d.sub.6, 400 MHz) .delta. 7.85 (d, J=8.4 Hz, 2H), 7.40-7.35
(m, 2H), 5.82 (d, J=10.0 Hz, 1H), 4.60-4.53 (m, 2H), 3.46-3.37 (m,
2H), 3.22 (s, 4H), 3.16 (d, J=13.2 Hz, 1H), 3.09-3.00 (m, 2H), 2.89
(s, 1H), 2.76 (d, J=12.8 Hz, 1H), 2.50-2.44 (m, 3H), 2.43-2.33 (m,
2H), 2.07-1.91 (m, 3H), 1.54-1.44 (m, 3H), 1.22-1.00 (m, 12H), 0.73
(d, J=6.4 Hz, 3H).
[0329] Na.sub.2CO.sub.3 (286.3 mg, 2.7 mmol, 3.0 eq) was added to a
solution of
(3R,3aS,4R,5R,7R,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-7-((methylthi-
o)methyl)-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)-
acetate (523.00 mg, 900.50 umol, 1.0 eq) and
7-fluoro-1-hydroxy-3H-2,1-benzoxaborol-6-ol (151.2 mg, 900.5 umol,
1.00 eq) in DMSO (20 mL). The mixture was stirred at 30-40.degree.
C. for 12 hours. The reaction was quenched by addition of 50 mL
water, and adjusted by addition of 2N HCl till pH<4, white solid
was precipitated and filtered to give crude
(3R,3aS,4R,5R,7R,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-7-((methylthi-
o)methyl)-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-
-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (520.0
mg, crude) as yellow solid.
[0330] ZnCl.sub.2 saturated in Con HCl (867.3 umol, 15.0 mL, 1.0
eq) was added to a solution of
(3R,3aS,4R,5R,7R,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-7-((methylthi-
o)methyl)-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-
-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (500.0
mg, 867.3 umol, 1.0 eq) in THE (20.0 mL) at 20.degree. C. for 12
hours. The reaction was treated with water 50 mL and 50 mL DCM. The
aqueous solution was treated with DCM (30 mL.times.3). The combined
organic phase was dried over Na.sub.2SO.sub.4 and concentrated in
vacuo. The crude product was purified by prep-HPLC ((column: Luna
C18 100.times.30 mm, 5 .mu.m; liquid phase: [A-TFA/H.sub.2O=0.075%
v/v; B-ACN, B %: 30%-60%, 12 min]). The solvent was concentrated to
30 mL solution left and lyophilized to give
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-((meth-
ylthio)methyl)-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-f-
luoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(71.0 mg, 123.9 umol, 14.3% yield, 98.1% purity) as white solid
.sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 9.28 (s, 1H), 7.25 (t,
J=8.0 Hz, 1H), 7.09 (d, J=8.0 Hz, 1H), 5.64 (d, J=7.6 Hz, 1H), 4.92
(s, 2H), 4.84-4.71 (m, 2H), 3.40 (d, J=6.0 Hz, 1H), 2.83-2.62 (m,
2H), 2.37 (br. s., 1H), 2.22-1.99 (m, 3H), 1.86 (s, 4H), 1.72-1.37
(m, 6H), 1.34-1.20 (m, 5H), 0.97-0.95 (m, 4H), 0.82 (d, J=7.2 Hz,
3H), 0.63 (d, J=6.4 Hz, 3H). MS (ESI): mass calcd. for
C.sub.29H.sub.40BFO.sub.7S 562.26, m/z found 561.2 [M-H].sup.-.
HPLC: 98.14% (220 nm), 94.91% (254 nm). and
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-((methylsul-
finyl)methyl)-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fl-
uoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(96.0 mg, 154.7 umol, 17.8% yield, 93.2% purity) as white solid.
.sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 7.46-7.22 (m, 1H),
7.16-7.05 (m, 1H), 5.85 (s, 1H), 5.46 (d, J=8.0 Hz, 1H), 4.99-4.59
(m, 5H), 3.36 (d, J=5.6 Hz, 2H), 2.99-2.79 (m, 2H), 2.43 (br. s.,
1H), 2.35 (s, 2H), 2.24-1.98 (m, 4H), 1.80-1.12 (m, 12H), 1.03 (d,
J=8.4 Hz, 1H), 0.83 (d, J=6.4 Hz, 3H), 0.63 (d, J=7.2 Hz, 3H). MS
(ESI): mass calcd. for C.sub.29H.sub.40BFO.sub.8S 578.25, m/z found
577 [M-H].sup.-. HPLC: 93.2% (220 nm), 89.9% (254 nm). [0331] 31.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-formyl-8-hydroxy-4,7,9,12-tetramethyl-3-ox-
odecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3-
-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate [0332] 32.
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-((methylami-
no)methyl)-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluor-
o-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
[0333] 33.
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-((dimethylamino)methyl)-8-hydroxy-4,7,9,12-
-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-flu-
oro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
[0334] 34.
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-((ethylamino)methyl)-8-hydroxy-4,7,9,12-te-
tramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-
-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate [0335]
35.
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-7-((pro-
pylamino)methyl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluor-
o-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
[0336] 36.
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-((butylamino)methyl)-8-hydroxy-4,7,9,12-te-
tramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-
-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate [0337]
37.
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-((cyclopropylamino)methyl)-8-hydroxy-4,7,9-
,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7--
fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00137## ##STR00138##
[0338]
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-formyl-8-hydroxy-4,7,9,12-tetramethy-
l-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(tosyloxy)acetate
(300.0 mg, 561.1 umol, 1.0 eq),
7-fluoro-1-hydroxy-3H-2,1-benzoxaborol-6-ol (94.2 mg, 561.1 umol,
1.0 eq) and Na.sub.2CO.sub.3 (178.41 mg, 1.68 mmol, 3.00 eq) in
DMSO (10.0 mL) were heated to 30-40.degree. C. for 12 hours. 20 mL
water was added to the mixture, white solid precipitated and
filtered to give crude product. The crude product was purified by
prep-HPLC (column: Luna C18 100.times.30 mm, 5 .mu.m; liquid phase:
[A-TFA/H.sub.2O=0.075% v/v; B-ACN]B %: 33%-53%, 12 min]) to give
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-formyl-8-hydroxy-4,7,9,12-tetramethyl-3-ox-
odecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3-
-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (81.0 mg, 152.7
umol, 27.2% yield, 10% purity) as white solid. .sup.1H NMR
(DMSO-d.sub.6, 400 MHz) .delta. 9.67 (s, 1H), 9.27 (s, 1H), 7.24
(t, J=7.9 Hz, 1H), 7.11 (d, J=8.4 Hz, 1H), 5.42 (d, J=8.4 Hz, 1H),
4.92 (s, 2H), 4.86-4.75 (m, 3H), 3.57 (t, J=6.6 Hz, 1H), 2.43-2.03
(m, 4H), 1.76-1.21 (m, 10H), 1.09 (s, 3H), 0.95 (d, J=7.1 Hz, 3H),
0.89-0.80 (m, 2H), 0.62 (d, J=7.1 Hz, 3H). MS (ESI): mass calcd.
for C.sub.28H.sub.36BFO.sub.8 530.3, m/z found 529.3 [M-H].sup.-.
HPLC: 100% in 220 nm; 100% in 254 nm.
[0339] NaBH.sub.3CN (142.2 mg, 2.3 mmol, 4.0 eq) was added to a
solution of
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-formyl-8-hydroxy-4,7,9,12-tetramethyl-3-
-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydroxy--
1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (300.0 mg, 565.6
umol, 1.0 eq) and Amine (4.0 eq) in MeOH (10.0 mL) and AcOH (1.0
mL). The mixture was stirred at 15.degree. C. for 12 hours. 30 mL
water was added to the mixture, and the mixture was treated with
DCM (30 mL.times.3). The combined organic phase was concentrated to
give crude product. The crude product was purified by
prep-HPLC.
[0340]
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-((met-
hylamino)methyl)-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-
-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate:
Prep-HPLC conditions: (column: Luna C18 100.times.30 mm, 5 .mu.m;
liquid phase: [A-TFA/H.sub.2O=0.075% v/v; B-ACN]B %: 26%-46%, 12
min]). The solvent was concentrated to about 15-20 mL solution
left, and dried over lyophilizer to give
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-((methylami-
no)methyl)-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluor-
o-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (52.0
mg, 95.3 umol, 16.8% yield) as white TFA salt solid. .sup.1H NMR
DMSO-d.sub.6, (400 MHz) .delta. 9.30 (br. s., 1H), 8.01 (br. s.,
2H), 7.31 (t, J=8.0 Hz, 1H), 7.13 (d, J=7.8 Hz, 1H), 5.36 (d, J=8.0
Hz, 1H), 4.93 (s, 2H), 4.87-4.71 (m, 2H), 3.47 (d, J=5.3 Hz, 1H),
3.27 (d, J=8.8 Hz, 1H), 3.12 (d, J=10.5 Hz, 1H), 2.62-2.57 (m, 3H),
2.26-1.93 (m, 6H), 1.71-1.21 (m, 10H), 1.14-0.94 (m, 4H), 0.84 (d,
J=6.3 Hz, 3H), 0.64 (d, J=7.0 Hz, 3H). MS (ESI): mass calcd. for
C.sub.31H.sub.42BF.sub.4NO.sub.9 545.3 m/z found 546.3 [M+H].sup.+.
HPLC: 96.4% in 220 nm; 100% in 254 nm.
[0341]
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-((dimethylamino)methyl)-8-hydroxy-4,-
7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-(-
(7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate:
Prep-HPLC conditions: (column: Waters Xbridge Prep OBD 100.times.19
mm, 5 .mu.m; liquid phase: [A-TFA/H.sub.2O=0.075% v/v; B-ACN]B %:
22%-52%, 3 min]). The solvent was concentrated to about 20 mL
solution left, and dried over lyophilizer to give
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-((dimethylamino)methyl)-8-hydroxy-4,7,9,12-
-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-flu-
oro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(64.0 mg, 114.4 umol, 20.2% yield) as white TFA salt solid. .sup.1H
NMR (DMSO-d.sub.6, 400 MHz) .delta. 9.29 (br. s., 1H), 8.81 (br.
s., 1H), 7.27 (t, J=7.7 Hz, 1H), 7.12 (d, J=8.4 Hz, 1H), 5.94 (br.
s., 1H), 5.35 (d, J=7.9 Hz, 1H), 4.93 (s, 2H), 4.83 (br. s., 2H),
3.72-3.40 (m, 4H), 3.10 (d, J=13.2 Hz, 1H), 2.86-2.84 (m, 4H), 2.41
(br. s., 1H), 2.27-1.99 (m, 4H), 1.77-1.18 (m, 12H), 1.12-0.96 (m,
2H), 0.88 (d, J=6.2 Hz, 3H), 0.65 (d, J=5.7 Hz, 3H). MS (ESI): mass
calcd. for C.sub.32H.sub.44BF.sub.4NO.sub.9 559.3 m/z found 560.3
[M+H].sup.+. HPLC: 96.8% in 220 nm; 100% in 254 nm.
[0342]
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-((ethylamino)methyl)-8-hydroxy-4,7,9-
,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7--
fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate:
Prep-HPLC conditions: (column: Luna C18 100.times.30 mm, 5 .mu.m;
liquid phase: [A-TFA/H.sub.2O=0.075% v/v; B-ACN]B %: 10%-45%, 12
min]). The solvent was concentrated to about 20 mL left, and dried
over lyophilizer to give
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-((ethylamino)methyl)-8-hydroxy-4,7-
,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((-
7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(109.0 mg, 191.4 umol, 33.8% yield, 98.2% purity) as white TFA salt
solid. .sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 9.28 (br. s.,
1H), 7.88 (br. s., 1H), 7.73 (br. s., 1H), 7.31 (t, J=8.2 Hz, 1H),
7.12 (d, J=8.4 Hz, 1H), 5.42 (br. s., 1H), 5.36 (d, J=8.4 Hz, 1H),
4.93 (s, 2H), 4.86-4.74 (m, 2H), 3.49 (d, J=5.7 Hz, 1H), 3.33-3.22
(m, 1H), 3.14-2.94 (m, 3H), 2.42 (br. s., 1H), 2.25-1.94 (m, 4H),
1.72-0.94 (m, 18H), 0.84 (d, J=7.1 Hz, 2H), 0.64 (d, J=7.1 Hz, 3H).
MS (ESI): mass calcd. for C.sub.32H.sub.44BF.sub.4NO.sub.9 559.3
m/z found 560.3 [M+H].sup.+. HPLC: 98.2% in 220 nm; 100% in 254
nm.
[0343]
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-7-
-((propylamino)methyl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-
-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate:
Prep-HPLC conditions: (column: Luna C18 100.times.30 mm, 5 .mu.m;
liquid phase: [A-TFA/H.sub.2O=0.075% v/v; B-ACN]B %: 29%-49%, 12
min]). The solvent was concentrated to about 15-20 mL solution
left, and dried over lyophilizer to give
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-7-((pro-
pylamino)methyl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluor-
o-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(171.0 mg, 294.9 umol, 52.2% yield, 98.92% purity) as white TFA
salt solid. .sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 9.29 (br.
s., 1H), 7.96 (br. s., 2H), 7.77 (br. s., 1H), 7.31 (t, J=7.9 Hz,
1H), 7.11 (d, J=7.9 Hz, 1H), 5.48 (br. s., 1H), 5.35 (d, J=7.9 Hz,
1H), 4.93 (s, 2H), 4.87-4.75 (m, 2H), 3.49 (d, J=5.7 Hz, 1H), 3.29
(t, J=10.1 Hz, 1H), 3.17-3.04 (m, 1H), 2.97-2.82 (m, 2H), 2.41 (br.
s., 1H), 2.24-1.91 (m, 4H), 1.75-0.95 (m, 17H), 0.90-0.79 (m, 4H),
0.65 (d, J=7.1 Hz, 3H). MS (ESI): mass calcd. for
C.sub.33H.sub.46BF.sub.4NO.sub.9 573.3 m/z found 574.3 [M+H].sup.+.
HPLC: 98.9% in 220 nm; 100% in 254 nm.
[0344]
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-((cyclopropylamino)methyl)-8-hydroxy-
-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl-
2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate:
Prep-HPLC conditions: (column: Luna C18 100.times.30 mm, 5 .mu.m;
liquid phase: [A-TFA/H.sub.2O=0.075% v/v; B-ACN]B %: 27%-47%, 12
min]). The solvent was concentrated to about 15-20 mL solution
left, and dried over lyophilizer to give
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-((cyclopropylamino)methyl)-8-hydroxy-4,7,9-
,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7--
fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(129.0 mg, 220.5 umol, 39.0% yield, 97.7% purity) as white TFA salt
solid. .sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 9.29 (br. s.,
1H), 8.29 (br. s., 1H), 7.99 (br. s., 1H), 7.32 (t, J=8.2 Hz, 1H),
7.12 (d, J=7.9 Hz, 1H), 5.42 (d, J=8.4 Hz, 2H), 4.93 (s, 2H),
4.87-4.75 (m, 2H), 3.48 (d, J=6.2 Hz, 1H), 3.39-3.22 (m, 2H), 2.73
(br. s., 1H), 2.42 (br. s., 1H), 2.25-1.91 (m, 5H), 1.74-1.22 (m,
10H), 1.13-0.92 (m, 6H), 0.89-0.68 (m, 6H), 0.65 (d, J=7.1 Hz, 3H).
MS (ESI): mass calcd. for C.sub.33H.sub.44BF.sub.4NO.sub.9 571.3
m/z found 572.3 [M+H].sup.+. HPLC: 97.7% in 220 nm; 100% in 254
nm.
[0345]
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-((butylamino)methyl)-8-hydroxy-4,7,9-
,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7--
fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate:
Prep-HPLC conditions: (column: Luna C18 100.times.30 mm, 5 .mu.m;
liquid phase: [A-TFA/H.sub.2O=0.075% v/v; B-ACN]B %: 32%-52%, 12
min]). The solvent was concentrated to about 15-20 mL solution
left, and dried over lyophilizer to give
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-((butylamino)methyl)-8-hydroxy-4,7,9,12-te-
tramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-
-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (111.0
mg, 186.2 umol, 49.4% yield, 98.6% purity) as white TFA salt solid.
.sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 9.28 (br. s., 1H), 7.97
(br. s., 1H), 7.76 (br. s., 1H), 7.31 (t, J=8.2 Hz, 1H), 7.11 (d,
J=7.9 Hz, 1H), 5.35 (d, J=8.4 Hz, 1H), 4.92 (s, 2H), 4.86-4.75 (m,
2H), 3.49 (d, J=6.2 Hz, 1H), 3.28 (t, J=9.9 Hz, 1H), 3.18-3.06 (m,
1H), 2.93 (br. s., 2H), 2.42 (br. s., 1H), 2.25-1.91 (m, 5H),
1.73-1.20 (m, 15H), 1.17-0.96 (m, 4H), 0.90-0.79 (m, 5H), 0.65 (d,
J=6.6 Hz, 3H). MS (ESI): mass calcd. for
C.sub.34H.sub.48BF.sub.4NO.sub.9 587.3 m/z found 588.5 [M+H].sup.+.
HPLC: 98.6% in 220 nm; 91.6% in 254 nm. [0346] 38.
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-(azetidin-1-ylmethyl)-8-hydroxy-4,7,9,12-t-
etramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluor-
o-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00139##
[0347] To a solution of
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-formyl-8-hydroxy-4,7,9,12-tetramethyl-3-ox-
odecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3-
-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (500.0 mg, 942.7
umol, 1.0 eq) in MeOH (10 mL) was added azetidine;hydrochloride
(441.0 mg, 4.71 mmol, 5.00 eq), CH.sub.3COOH (2.6 g, 43.7 mmol, 2.5
mL, 46 eq), NaBH.sub.3CN (237.0 mg, 3.8 mmol, 4.0 eq) and
sodium;triacetoxyboranuide (399.6 mg, 1.9 mmol, 2.0 eq) at
25.degree. C. The mixture was stirred at 25.degree. C. for 3 hrs.
HPLC showed the reaction was completed. H.sub.2O (20 mL) was added
to the mixture. The aqueous layer was extracted with DCM (20
mL.times.3). The combined organic layers were washed with brine (20
mL) and dried over Na.sub.2SO.sub.4. After filtration via filter
paper, the organic layer was concentrated under reduced pressure to
provide crude product, which was combined and purified by prep-HPLC
(column: Luna C8 100.times.30 mm, 5 .mu.m; liquid phase:
[A-TFA/H.sub.2O=0.075% v/v; B-ACN]B %: 25%-55%, 12 min]). After
prep-HIPLC purification, the eluent was concentrated to remove
organic solvent. The residual aqueous solution was lyophilized to
give
1-(((3aR,4R,5R,7S,8S,9R,9aS,12R)-5-(2-((7-fluoro-1-hydroxy-1,3-dihydroben-
zo[c][1,2]oxaborol-6-yl)oxy)acetoxy)-8-hydroxy-4,7,9,12-tetramethyl-3-oxod-
ecahydro-4,9a-propanocyclopenta[8]annulen-7-yl)methyl)azetidin-1-ium
2,2,2-trifluoroacetate (160.0 mg, 20.5% yield) as a white solid.
.sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 9.01 (br. s., 1H), 7.34
(t, J=8.0 Hz, 1H), 7.15 (d, J=8.0 Hz, 1H), 5.28 (d, J=8.0 Hz, 1H),
4.94 (s, 2H), 4.90-4.77 (m, 2H), 4.30-3.40 (m, 7H), 2.40 (s, 1H),
2.31-1.93 (m, 5H), 1.72-1.23 (m, 11H), 1.17-0.95 (m, 5H), 0.84 (d,
J=6.4 Hz, 3H), 0.65 (d, J=6.4 Hz, 3H). HPLC: 98.2% (220 nm), 100%
(254 nm). MS (ESI): mass calcd. for C.sub.31H.sub.43BFNO.sub.7
571.3, m/z found 572.4 [M+H].sup.+. [0348] 39.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-(2-(azetidin-1-yl)ethyl)-8-hydroxy-4,7-
,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((-
7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00140##
[0349] To a solution of
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-8-oxo-7-(2-ox-
oethyl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl
2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(300.0 mg, 537.2 umol, 1.0 eq) in MeOH (5.0 mL) was added
CH.sub.3COOH (525.0 mg, 8.7 mmol, 500.0 uL, 16.3 eq),
azetidine;hydrochloride (251.3 mg, 2.7 mmol, 5.0 eq), NaBH.sub.3CN
(135.0 mg, 2.2 mmol, 4.0 eq) and sodium triacetoxyboranuide (227.7
mg, 1.1 mmol, 2.0 eq) at 25.degree. C. The mixture was stirred at
25.degree. C. for 3 hrs. The mixture was added H.sub.2O (20 mL).
The aqueous phase was extracted with DCM (20 mL.times.3). The
combined organic phase was washed with brine (15 mL.times.2), dried
with anhydrous Na.sub.2SO.sub.4, filtered and concentrated in
vacuum to give compound
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-(2-(azetidin-1-yl)ethyl)-3-methoxy-4,7,9,1-
2-tetramethyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fl-
uoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(300.0 mg, crude) as a light yellow solid.
[0350] To a mixture of
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-(2-(azetidin-1-yl)ethyl)-3-methoxy-4,7,9,1-
2-tetramethyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fl-
uoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(300.0 mg, 500.4 umol, 1.0 eq) in THE (5.0 mL) was added ZnCl.sub.2
(29.1 mg, 10.0 mL, saturated in con.HCl) in one portion at
25.degree. C. The mixture was stirred at 25.degree. C. for 12 hrs.
HPLC and LCMS showed the reaction was complete. The mixture was
added H.sub.2O (20 mL). The aqueous phase was extracted with DCM
(20 mL.times.3). The combined organic phase was washed with brine
(10 mL.times.2), dried with anhydrous Na.sub.2SO.sub.4, filtered
and concentrated in vacuum to give crude product, which was
purified by prep-HPLC (column: Luna C18 100.times.30 mm, 5 .mu.m;
liquid phase: [A-HCl/H.sub.2O=0.040% v/v; B-ACN]B %: 16%-46%, 11
min]). After prep-HPLC purification, the eluent was concentrated to
remove organic solvent, and 0.2 mL of 4 N hydrochloride acid was
added, the residual aqueous solution was lyophilized to give
product
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-(2-(azetidin-1-yl)ethyl)-8-hydroxy-
-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl-
2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(83.0 mg, 131.2 umol, 26.2% yield, 98.3% purity) as white solid.
.sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 9.30 (br. s., 1H), 7.31
(t, J=8.0 Hz, 1H), 7.16 (d, J=8.0 Hz, 1H), 5.51 (d, J=8.0 Hz, 1H),
4.98-4.82 (m, 4H), 3.89-3.68 (m, 2H), 2.44-2.39 (m, 1H), 2.08 (m,
7H), 1.36 (s, 13H), 1.18-0.91 (m, 8H), 0.83 (d, J=6.5 Hz, 3H), 0.66
(d, J=6.5 Hz, 3H). MS (ESI): mass calcd. for
C.sub.32H.sub.46BClFNO.sub.7 621.3, m/z found 586.3 [M+H].sup.+.
HPLC: 98.3% (220 nm), 100% (254 nm). [0351] 40.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-7-(2-(p-
iperidin-1-yl)ethyl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-f-
luoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00141##
[0352] To a solution of
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-8-oxo-7-(2-ox-
oethyl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl
2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(300.0 mg, 537.2 umol, 1.0 eq) in MeOH (5.0 mL) was added
CH.sub.3COOH (525.0 mg, 8.7 mmol, 500.0 uL, 16.3 eq), sodium
triacetoxyboranuide (227.7 mg, 1.1 mmol, 2.0 eq) and piperidine
(228.7 mg, 2.7 mmol, 265.9 uL, 5.00 eq) at 25.degree. C. The
mixture was stirred at 25.degree. C. for 3 hrs. The mixture was
added H.sub.2O (20 mL). The aqueous phase was extracted with DCM
(20 mL.times.3). The combined organic phase was washed with brine
(15 mL.times.2), dried with anhydrous Na.sub.2SO.sub.4, filtered
and concentrated in vacuum to give compound
(3R,3aS,4R,5R,7R,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-8-oxo-7-(2-(p-
iperidin-1-yl)ethyl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl
2-((7-fluoro-1-hydroxy-1,3-dihydro
benzo[c][1,2]oxaborol-6-yl)oxy)acetate (300.0 mg, crude) as a light
yellow solid.
[0353] To a mixture of compound
(3R,3aS,4R,5R,7R,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-8-oxo-7-(2-(p-
iperidin-1-yl)ethyl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-f-
luoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(300.0 mg, 478.0 umol, 1.0 eq) in THE (5.0 mL) was added ZnCl.sub.2
(29.1 mg, 10.0 mL, saturated in con.HCl) in one portion at
25.degree. C. The mixture was stirred at 25.degree. C. for 12 hrs.
HPLC and LCMS showed the reaction was complete. The mixture was
added H.sub.2O (20 mL). The aqueous phase was extracted with DCM
(20 mL.times.3). The combined organic phase was washed with brine
(10 mL.times.2), dried with anhydrous Na.sub.2SO.sub.4, filtered
and concentrated in vacuum to give crude product, which was
purified by prep-HPLC (column: Luna C18 100.times.30 mm, 5 .mu.m;
liquid phase: [A-HCl/H.sub.2O=0.040% v/v; B-ACN]B %: 19%-49%, 11
min]). After prep-HPLC purification, the eluent was concentrated to
remove organic solvent. The residual aqueous solution was
lyophilized to give
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-3-oxo-7-(2-(p-
iperidin-1-yl)ethyl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl
2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)
acetate (160.0 mg, 240.3 umol, 50.3% yield, 97.6% purity) as
colorless oil. .sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 9.27
(br. s., 1H), 7.28 (t, J=8.2 Hz, 1H), 7.12 (d, J=7.9 Hz, 1H), 5.46
(d, J=8.4 Hz, 1H), 4.95-4.77 (m, 4H), 3.62 (t, J=6.6 Hz, 5H), 2.05
(s, 2H), 1.95 (br. s., 1H), 1.81-1.68 (m, 6H), 1.66-1.53 (m, 9H),
1.51-1.24 (m, 9H), 0.97-0.88 (m, 3H), 0.81 (d, J=7.1 Hz, 3H), 0.64
(d, J=6.6 Hz, 3H). MS (ESI): mass calcd. for
C.sub.34H.sub.50BClFNO.sub.7 649.3, m/z found 614.5 [M+H].sup.+.
HPLC: 97.6% (220 nm), 100% (254 nm). [0354] 41.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-(2-morpholi-
noethyl)-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl
2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00142##
[0355] NaBH.sub.3CN (112.5 mg, 1.8 mmol, 4.0 equiv) was added to a
solution of
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-8-oxo-7-(2-ox-
oethyl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydro-
xy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (250.0 mg,
447.7 umol, 1.0 equiv) and morpholine (195.0 mg, 2.2 mmol, 196.9
uL, 5.0 equiv) in MeOH (20.0 mL) and AcOH (1.0 mL). The mixture was
stirred at 20.degree. C. for 12 hours. HPLC and LCMS showed major
as desired. The mixture was treated with DCM 50 mL and water 100
mL. The aqueous phase was treated with DCM (50 mL.times.3). The
combined organic phase was dried over Na.sub.2SO.sub.4 and
concentrated in vacuo to give
(3R,3aS,4R,5R,7R,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-7-(2-morpholi-
noethyl)-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro--
1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (180.0
mg, 285.9 umol, 63.9% yield) as yellow oil. MS (ESI): mass calcd.
For C.sub.34H.sub.49BFNO.sub.8 629.3, m/z found 630 [M+H].sup.+
[0356] ZnCl.sub.2 in saturated con.HCl (285.9 umol, 5.0 mL, 1.0
equiv) was added to a solution of
(3R,3aS,4R,5R,7R,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-7-(2-morpholi-
noethyl)-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro--
1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (180.0
mg, 285.9 umol, 1.0 equiv) in THE (15.0 mL) at 20.degree. C. and
stirred at 20.degree. C. for 12 hours. The mixture was treated with
DCM 50 mL and water 50 mL, the aqueous phase was extracted with DCM
(30 mL.times.3). The organic phase was dried over Na.sub.2SO.sub.4
and concentrated in vacuo. The crude product was purified by
prep-HPLC ((column: Luna C18 100.times.30 mm, 5 .mu.m; liquid
phase: [A-TFA/H.sub.2O=0.075% v/v; B-ACN]B %: 25%-65%, 12 min])).
The mixture was concentrated in vacuo till 20 mL solution left and
0.2 mL of 4 N hydrochloride acid was added, then the mixture was
lyophilized to give
(3aR,4R,5R,7R,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-(2-morpholi-
noethyl)-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro--
1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (96.0
mg, 158.4 umol, 55.4% yield, 97.2% purity) as white solid. .sup.1H
NMR (DMSO-d.sub.6, 400 MHz) .delta. 10.20 (br. s., 1H), 9.28 (s,
1H), 7.31 (t, J=7.5 Hz, 1H), 7.15 (d, J=8.0 Hz, 1H), 5.52 (d, J=8.0
Hz, 1H), 5.02-4.74 (m, 4H), 4.38 (t, J=5.0 Hz, 2H), 3.64 (t, J=6.8
Hz, 2H), 3.41-3.34 (m, 4H), 2.40 (br. s., 1H), 2.25-1.85 (m, 3H),
1.81-1.70 (m, 4H), 1.69-1.39 (m, 9H), 1.34 (s, 4H), 0.97 (s, 3H),
0.93 (s, 3H), 0.83 (d, J=7.0 Hz, 3H), 0.64 (d, J=7.0 Hz, 3H). MS
(ESI): mass calcd. for C.sub.33H.sub.48BClFNOs 651.3, m/z found
616.3 [M+H].sup.+ HPLC: 97.2% (220 nm); 100% (254 nm). [0357] 42.
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-(2-(diethylamino)ethyl)-8-hydroxy-4,7,9,12-
-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-flu-
oro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00143##
[0358] To a solution of
(3R,3aS,4R,5R,7S,9R,9aR,12R)-3-methoxy-4,7,9,12-tetramethyl-8-oxo-7-(2-ox-
oethyl)decahydro-4,9a-propanocyclopenta[8]annulen-5-yl
2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(300.0 mg, 537.2 umol, 1.0 eq) in MeOH (5.0 mL) was CH.sub.3COOH
(525.0 mg, 8.7 mmol, 500.0 uL, 16.3 eq), N-ethylethanamine
hydrochloride (294.4 mg, 2.7 mmol, 5.0 eq) and sodium
triacetoxyboranuide (227.7 mg, 1.1 mmol, 2.0 eq) at 25.degree. C.
The mixture was stirred at 25.degree. C. for 3 hrs. The mixture was
added H.sub.2O (20 mL). The aqueous phase was extracted with DCM
(20 mL.times.3). The combined organic phase was washed with brine
(15 mL.times.2), dried with anhydrous Na.sub.2SO.sub.4, filtered
and concentrated in vacuum to give
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-(2-(diethylamino)ethyl)-3-methoxy-4,7,9,12-
-tetramethyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-flu-
oro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(300.0 mg, crude) as a light yellow solid.
[0359] To a mixture of
(3R,3aS,4R,5R,7R,9R,9aR,12R)-7-(2-(diethylamino)ethyl)-3-methoxy-4,7,9,12-
-tetramethyl-8-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-flu-
oro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(300.0 mg, 487.4 umol, 1.0 eq) in THE (5.0 mL) was added ZnCl.sub.2
(29.1 mg, 10.0 mL, saturated in con.HCl) in one portion at
25.degree. C. The mixture was stirred at 25.degree. C. for 12 hrs.
HPLC and LCMS showed the reaction was complete. The mixture was
added H.sub.2O (20 mL). The aqueous phase was extracted with DCM
(20 mL.times.3). The combined organic phase was washed with brine
(10 mL.times.2), dried with anhydrous Na.sub.2SO.sub.4, filtered
and concentrated in vacuum to give crude product, which was
purified by prep-HPLC (column: Luna C18 100.times.30 mm, 5 .mu.m;
liquid phase: [A-HCl/H.sub.2O=0.040% v/v; B-ACN]B %: 23%-53%, 11
min]). After prep-HPLC purification, the eluent was concentrated to
remove organic solvent. The residual aqueous solution was
lyophilized to give
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-(2-(diethylamino)ethyl)-8-hydroxy-4,7,9,12-
-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-flu-
oro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(62.0 mg, 93.7 umol, 19.2% yield, 96.5% purity) as white solid.
.sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 7.21 (br. s., 1H), 7.08
(d, J=7.5 Hz, 1H), 4.89 (s, 3H), 4.80 (br. s., 2H), 4.38-4.28 (m,
3H), 3.62 (t, J=6.6 Hz, 4H), 1.78-1.66 (m, 3H), 1.65-1.53 (m, 4H),
1.53-1.36 (m, 9H), 1.35-1.21 (m, 3H), 0.97-0.76 (m, 12H), 0.62 (d,
J=6.6 Hz, 3H). MS (ESI): mass calcd. for
C.sub.33H.sub.50BClFNO.sub.7 637.3 m/z found 602.4 [M+H].sup.+.
HPLC: 96.5% (220 nm), 100% (254 nm). [0360] 43.
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-7-((hydroxyimino)methyl)-4,7,9,12--
tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluo-
ro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00144##
[0361]
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-formyl-8-hydroxy-4,7,9,12-tetramethy-
l-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydro-
xy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (400.0 mg,
754.2 umol, 1.0 eq) and NH.sub.2OH.HCl (62.9 mg, 905.0 umol, 1.2
eq) in H.sub.2O (5.0 mL) and EtOH (10.0 mL) were stirred at
15.degree. C. for 12 hours. HPLC and LCMS showed major as desired,
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-formyl-8-hydroxy-4,7,9,12-tetramethyl-3-ox-
odecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3-
-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate consumed. 30 mL
water was added to the mixture, white solid precipitated, the
mixture was filtered to give crude product. The crude product was
purified by prep-HPLC (column: Luna C8 100.times.30 mm, 5 .mu.m;
liquid phase: [A-TFA/H.sub.2O=0.075% v/v; B-ACN]B %: 30%-50%, 12
min]). The solvent was concentrated to about 15 mL solution left,
and dried by lyophilizer to give
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-7-((hydroxyimino)methyl)-4,7,-
9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-
-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(99.0 mg, 174.3 umol, 23.1% yield, 96.0% purity) as white solid.
.sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 10.41 (br. s., 1H),
9.25 (br. s., 1H), 7.51 (s, 1H), 7.23 (t, J=7.9 Hz, 1H), 7.10 (d,
J=7.9 Hz, 1H), 5.55 (d, J=7.9 Hz, 1H), 4.92 (s, 2H), 4.78 (s, 2H),
3.46 (d, J=6.6 Hz, 1H), 2.41 (br. s., 1H), 2.25-2.01 (m, 3H),
1.75-0.94 (m, 16H), 0.85 (d, J=7.1 Hz, 3H), 0.62 (d, J=6.6 Hz, 3H).
MS (ESI): mass calcd. for C.sub.28H.sub.37BFNO.sub.8 545.26 m/z
found 546.3 [M+H].sup.+. HPLC: 96.2% in 220 nm; 100% in 254 nm.
[0362] 44.
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-7-((methoxyimino)methyl)-4,7,9,12--
tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluo-
ro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00145##
[0363] To a mixture of
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-formyl-8-hydroxy-4,7,9,12-tetramethyl-3-ox-
odecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3-
-dihydroben zo[c][1,2]oxaborol-6-yl)oxy)acetate (150.0 mg, 282.8
umol, 1.0 eq.) and O-methyl hydroxylamine (35.4 mg, 424.2 umol, 1.5
eq., HCl) in EtOH (5.0 mL) and water (10.0 mL) was stirred for 12
hours at 25.degree. C. LC-MS showed the reaction was completed and
one main peak with desired MS was detected. The reaction mixture
was diluted with EtOAc 20 mL and extracted with EtOAc (10
mL.times.2). The combined organic layers were washed with brine 15
mL, dried over Na.sub.2SO.sub.4, filtered and concentrated under
reduced pressure to give a residue, which was purified by prep-HPLC
(column: Luna 100.times.30.0 mm, 5 .mu.m; liquid phase:
[A-H.sub.2O+0.075% TFA; B-ACN]B %: 47%-67%, 12 min]) to afford
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-7-((methoxyimino)methyl)-4,7,9,12--
tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluo-
ro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(50.0 mg, 89.4 umol, 31.6% yield) as a white solid. .sup.1H NMR
(DMSO-d.sub.6, 400 MHz) .delta. 9.25 (br. s., 1H), 7.50 (s, 1H),
7.25 (t, J=8.0 Hz, 1H), 7.10 (d, J=8.4 Hz, 1H), 5.60 (d, J=8.0 Hz,
1H), 4.92 (s, 2H), 4.78 (s, 2H), 3.62 (s, 3H), 3.48 (d, J=5.6 Hz,
1H), 2.41 (br. s., 1H), 2.24-1.97 (m, 4H), 1.72-1.40 (m, 5H),
1.35-1.19 (m, 5H), 1.15-0.96 (m, 5H), 0.85 (d, J=6.4 Hz, 3H), 0.63
(d, J=5.6 Hz, 3H) MS (ESI): mass calcd. for
C.sub.29H.sub.39BFNO.sub.8 559.28, m/z found 560.3 [M+H].sup.+.
HPLC: 97.5% (220 nm), 100.0% (254 nm). [0364] 45.
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-7-((methoxyamino)methyl)-4,7,9,12--
tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluo-
ro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00146##
[0365] To a mixture of
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-formyl-8-hydroxy-4,7,9,12-tetramethyl-3-ox-
odecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3-
-dihydro benzo[c][1,2]oxaborol-6-yl)oxy)acetate (150.0 mg, 282.8
umol, 1.0 eq.) and O-methyihydroxylamine (35.43 mg, 424.2 umol, 1.5
eq., HCl) in EtOH (5.0 mL) and water (10.0 mL) was stirred for 12
hours at 25.degree. C. LC-MS showed the reaction was completed and
one main peak with desired MS was detected. The reaction mixture
was diluted with EtOAc 20 mL and extracted with EtOAc (10
mL.times.2). The combined organic layers were washed with brine 15
mL, dried over Na.sub.2SO.sub.4, filtered and concentrated under
reduced pressure to give a residue, which was purified by prep-HPLC
(column: Luna 100.times.30.0 mm, 5 .mu.m; liquid phase:
[A-H.sub.2O+0.075% TFA; B-ACN]B %: 47%-67%, 12 min]) to afford
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-7-((Z)-(methoxyimino)methyl)-4,7,9-
,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7--
fluoro-1-hydroxy-1,3-dihy-drobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(50.0 mg, 89.4 umol, 31.6% yield) as a white solid. .sup.1H NMR
(DMSO-d.sub.6, 400 MHz) .delta. 9.24 (br. s., 1H), 7.50 (s, 1H),
7.25 (t, J=8.0 Hz, 1H), 7.10 (d, J=8.0 Hz, 1H), 5.60 (d, J=8.0 Hz,
1H), 4.92 (s, 2H), 4.78 (s, 2H), 3.62 (s, 3H), 3.48 (d, J=6.4 Hz,
1H), 2.40 (br. s., 1H), 2.24-1.98 (m, 4H), 1.74-1.42 (m, 5H),
1.38-1.17 (m, 6H), 1.10-0.98 (m, 4H), 0.85 (d, J=7.2 Hz, 3H), 0.62
(d, J=6.4 Hz, 3H). MS (ESI): mass calcd. for
C.sub.29H.sub.39BFNO.sub.8 559.28, m/z found 560.3 [M+H].sup.+.
HPLC: 97.5% (220 nm), 100.0% (254 nm).
[0366] To a solution of
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-7-((Z)-(methoxyimino)
methyl)-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annu-
len-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)a-
cetate (1.0 g, 1.8 mmol, 1.0 eq.) in EtOH (15.0 mL) was added
pyridin-1-ium-1-ylboranuide (1.7 g, 17.9 mmol, 10.0 eq.).
Subsequently, MeOH/HCl (4 M, 8.0 mL, 17.9 eq.) was added under
N.sub.2 atmosphere at 0.degree. C. The mixture was stirred at
25.degree. C. for 12 hours. The mixture was adjusted to pH-6 with
saturated NaHCO.sub.3 and extracted with ethyl acetate (20
mL.times.2). After concentrated in vacuo, the residue was purified
by prep-HPLC (column: Luna 250.times.50.0 mm, 10 .mu.m; liquid
phase: [A-H.sub.2O=0.075% TFA; B-ACN]B %: 20%-50%, 20 min]) to
afford
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-7-((methoxyamino)methyl)-
-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl-
2-((7-fluoro-1-hydroxy-1,3-dihydro-benzo[c][1,2]oxaborol-6-yl)oxy)acetate
(432.0 mg, 769.4 umol, 43.0% yield) as a white solid. .sup.1H NMR
(DMSO-d.sub.6, 400 MHz) .delta. 7.28 (t, J=8.0 Hz, 1H), 7.12 (d,
J=8.0 Hz, 1H), 5.45-5.36 (m, 1H), 4.93 (s, 2H), 4.81 (d, J=2.4 Hz,
2H), 4.31 (d, J=5.6 Hz, 1H), 3.77-3.71 (m, 4H), 3.50-3.44 (m, 1H),
3.26 (t, J=13.2 Hz, 1H), 2.40 (br. s., 1H), 2.23-1.93 (m, 4H),
1.77-1.23 (m, 10H), 1.19-0.97 (m, 4H), 0.87 (d, J=6.4 Hz, 3H), 0.65
(dd, J=3.2, 6.8 Hz, 3H). MS (ESI): mass calcd. for
C.sub.31H.sub.42BF.sub.4NO.sub.10 561.29, m/z found 562.4
[M+H].sup.+. HPLC: 95.4% (220 nm), 95.1% (254 nm). [0367] 46.
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-7-((isopropoxyimino)methyl)-4,7,9,-
12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-f-
luoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00147##
[0368] A mixture of
(3aR,4R,5R,7R,8S,9R,9aS,12R)-7-formyl-8-hydroxy-4,7,9,12-tetramethyl-3-ox-
odecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3-
-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (400.0 mg, 754.2
umol, 1.0 eq.), O-isopropylhydroxylamine (100.0 mg, 905.0 umol, 1.2
eq, HCl) in EtOH (15.0 mL) and H.sub.2O (10.0 mL) was degassed and
purged with N.sub.2 for 3 times, and then the mixture was stirred
at 25.degree. C. for 12 hours under N.sub.2 atmosphere. The
reaction mixture was diluted with EtOAc 20 mL and extracted with
EtOAc (10 mL.times.2). The combined organic layers were washed with
brine 15 mL, dried over Na.sub.2SO.sub.4, filtered and concentrated
under reduced pressure to give a residue, which was purified by
prep-HPLC (column: Luna 250.times.50.0 mm, 10 .mu.m; liquid phase:
[A-H.sub.2O=0.075% TFA; B-ACN]B %: 40%-70%, 20 min]) to afford
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-7-((isoprop-oxyimino)methyl-
)-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-y-
l2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(139.00 mg, 233.65 umol, 30.98% yield, 98.75% purity) as a white
solid. .sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 9.26 (br. s.,
1H), 7.47 (s, 1H), 7.23 (t, J=8.0 Hz, 1H), 7.10 (d, J=8.0 Hz, 1H),
5.57 (d, J=8.0 Hz, 1H), 4.92 (s, 1H), 4.76 (s, 1H), 4.16 (dt,
J=5.6, 12.1 Hz, 1H), 3.48 (d, J=5.2 Hz, 2H), 2.41 (br. s., 1H),
2.09 (d, J=15.6 Hz, 4H), 1.73-1.21 (m, 12H), 1.19-0.97 (m, 10H),
0.86 (d, J=6.4 Hz, 3H), 0.63 (d, J=6.4 Hz, 3H). MS (ESI): mass
calcd. for C.sub.31H.sub.43BFNO.sub.8 587.48, m/z found 586.3
[M-H].sup.-. HPLC: 98.8% (220 nm), 85.1% (254 nm). [0369] 47.
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-(aminomethyl)-8-hydroxy-4,7,9,12-tetrameth-
yl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydr-
oxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate [0370] 48.
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-(acetamidomethyl)-8-hydroxy-4,7,9,12-tetra-
methyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1--
hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00148##
[0371] To a solution of
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-7-((hydroxyimino)methyl)-4,7,9,12--
tetramethyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluo-
ro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(570.0 mg, 1.0 mmol, 1.0 eq) in MeOH (10.0 mL) was added Ra--Ni
(0.5 g) under N.sub.2 atmosphere. The suspension was degassed and
purged with H.sub.2 for 3 times. The mixture was stirred under
H.sub.2 (50 psi) at 25.degree. C. for 2 hours. The reaction mixture
was filtered and the filter was concentrated to give a residue,
which was purified by prep-HPLC (column: Luna 250.times.50.0 mm, 10
.mu.m; liquid phase: [A-H.sub.2O+0.075% TFA; B-ACN]B %: 15%-45%, 20
min]) to give
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-(aminomethyl)-8-hydroxy-4,7,9,12-tetrameth-
yl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydr-
oxy-1,3-dihydro benzo[c][1,2]oxaborol-6-yl)oxy)acetate (300.0 mg,
464.8 umol, 44.2% yield, TFA) as a light yellow solid. .sup.1H NMR
(DMSO-d.sub.6, 400 MHz) .delta. 9.27 (br. s., 1H), 7.55 (br. s.,
2H), 7.25 (t, J=7.6 Hz, 1H), 7.15-7.06 (m, 1H), 5.49-5.28 (m, 2H),
4.91 (br. s., 1H), 4.78 (br. s., 1H), 3.51 (br. s., 1H), 3.18 (br.
s., 1H), 2.92 (br. s., 1H), 2.42 (d, J=8.4 Hz, 2H), 2.25-1.90 (m,
4H), 1.69-1.21 (m, 10H), 1.04 (br. s., 3H), 0.84 (d, J=5.6 Hz, 2H),
0.64 (d, J=6.4 Hz, 3H) MS (ESI): mass calcd. for
C.sub.30H.sub.40BF.sub.4NO.sub.9 531.28, m/z found 532.3
[M+H].sup.+. HPLC: 97.1% (220 nm), 93.6% (254 nm).
[0372] A mixture of
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-(aminomethyl)-8-hydroxy-4,7,9,12-tetrameth-
yl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydr-
oxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (300.0 mg,
564.5 umol, 1.0 eq.), Ac20 (63.4 mg, 620.9 umol, 1.1 eq.), AcOH
(67.8 mg, 1.1 mmol, 2.0 eq.) in DCM (20.0 mL) was degassed and
purged with N.sub.2 for 3 times, and then the mixture was stirred
at 60.degree. C. for 12 hours under N.sub.2 atmosphere. LC-MS
showed
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-(aminomethyl)-8-hydroxy-4,7,9,12-tetrameth-
yl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydr-
oxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate was consumed
completely and one main peak with desired MS was detected. The
solvent was removed. The residue was purified by prep-HPLC (column:
Luna 250.times.50.0 mm, 10 .mu.m; liquid phase: [A-H.sub.2O+0.075%
TFA; B-ACN]B %: 25%-55%, 20 min]) to give
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-(acetamidomethyl)-8-hydroxy-4,7,9,12-tetra-
methyl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1--
hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (97.0 mg,
169.1 umol, 29.9% yield) was obtained as a white solid. .sup.1H NMR
(DMSO-d.sub.6, 400 MHz) .delta. 7.28 (t, J=8.4 Hz, 1H), 7.09 (d,
J=8.4 Hz, 1H), 7.00-6.94 (m, 1H), 5.51 (d, J=8.4 Hz, 1H), 4.90 (s,
2H), 4.85-4.74 (m, 2H), 3.60 (dd, J=6.4, 13.8 Hz, 1H), 3.43 (d,
J=5.6 Hz, 1H), 3.00 (dd, J=4.4, 13.8 Hz, 1H), 2.36 (br. s., 1H),
2.31 (br. s., 1H), 2.23-1.99 (m, 3H), 1.94-1.82 (m, 1H), 1.81-1.73
(m, 2H), 1.69-1.55 (m, 2H), 1.48 (br. s., 1H), 1.40-1.20 (m, 6H),
1.05-0.87 (m, 4H), 0.83 (d, J=6.4 Hz, 2H), 0.62 (d, J=6.4 Hz, 3H)
MS (ESI): mass calcd. for C.sub.30H.sub.41BFNO.sub.8 573.29, m/z
found 574.3 [M+H].sup.+. HPLC: 100.0% (220 nm), 100.0% (254 nm).
[0373] 49.
(3aR,4R,5R,7S,8S,9R,9aS,12R)-4,7,9,12-tetramethyl-7-(methylsulfonamidomet-
hyl)-8-((methylsulfonyl)oxy)-3-oxodecahydro-4,9a-propanocyclopenta[8]annul-
en-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)ac-
etate [0374] 50.
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-(aminomethyl)-4,7,9,12-tetramethyl-8-((met-
hylsulfonyl)oxy)-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-
-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
##STR00149##
[0375] To a solution of
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-(aminomethyl)-8-hydroxy-4,7,9,12-tetrameth-
yl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydr-
oxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (100.0 mg,
188.2 umol, 1.0 eq.) in THE (10.00 mL) was added Na.sub.2CO.sub.3
(79.8 mg, 752.7 umol, 4.0 eq.) and MsCl (43.1 mg, 376.4 umol, 2.0
eq.). The mixture was stirred at 0.degree. C. for 1 hour. The
reaction mixture was partitioned between EtOAc (10 mL) and water
(10 mL). The organic phase was separated, washed with brine (10
mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under
reduced pressure to give a residue, which was purified by prep-HPLC
(column: Luna 100.times.30.0 mm, 5 .mu.m; liquid phase:
[A-H.sub.2O+0.075% TFA; B-ACN]B %: 41%-61%, 12 min]) to give
(3aR,4R,5R,7S,8S,9R,9aS,12R)-4,7,9,12-tetramethyl-7-(methylsul
fonamidomethyl)-8-((methylsulfonyl)oxy)-3-oxodecahydro-4,9a-propanocyclop-
enta[8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-
-6-yl)oxy)acetate(19.0 mg, 27.6 umol, 14.7% yield) as a white
solid. .sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 9.27 (br. s.,
1H), 7.34 (t, J=8.2 Hz, 1H), 7.12 (d, J=8.4 Hz, 1H), 6.42-6.36 (m,
1H), 5.53 (d, J=8.4 Hz, 1H), 4.93 (s, 2H), 4.80 (d, J=3.6 Hz, 2H),
4.74 (d, J=7.2 Hz, 1H), 3.40 (s, 1H), 3.20 (s, 3H), 3.16-3.07 (m,
1H), 2.85 (s, 3H), 2.41-2.38 (m, 1H), 2.23-2.00 (m, 5H), 1.96-1.84
(m, 1H), 1.68 (d, J=12.8 Hz, 1H), 1.59-1.24 (m, 8H), 1.05 (s, 3H),
0.97 (d, J=6.6 Hz, 3H), 0.64 (d, J=7.2 Hz, 3H). MS (ESI): mass
calcd. for C.sub.30H.sub.43BFNO.sub.11S.sub.2 687.24, m/z found
686.3 [M-H].sup.-. HPLC: 94.2% (220 nm), 52.7% (Weak absorbtion at
254 nm).
[0376] To a solution of
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-(aminomethyl)-8-hydroxy-4,7,9,12-tetrameth-
yl-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydr-
oxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate (600.0 mg,
1.1 mmol, 1.0 eq.) in THE (20 mL) was added NaHCO.sub.3(284.8 mg,
3.4 mmol, 3.0 eq.) and MsCl (129.3 mg, 1.1 mmol, 1.0 eq.). The
mixture was stirred at -78.degree. C. for 1 hour. The reaction
mixture was quenched by addition water (15 mL), and then extracted
with EtOAc (15 mL.times.2). The combined organic layers were washed
with brine (15 mL), dried over Na.sub.2SO.sub.4, filtered and
concentrated under reduced pressure to give a residue, which was
purified by prep-HPLC (column: Luna 250.times.50.0 mm, 5 .mu.m;
liquid phase: [A-H.sub.2O+0.075% TFA; B-ACN]B %: 20%-50%, 20 min])
to give
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-(aminomethyl)-4,7,9,12-tetramethyl-8-((met-
hylsulfonyl)oxy)-3-oxodecahydro-4,9a-propanocyclopenta[8]annulen-5-yl2-((7-
-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(242.0 mg, 334.5 umol, 29.6% yield) as a white solid. .sup.1H NMR
(DMSO-d.sub.6, 400 MHz) .delta. 9.29 (s, 1H), 7.74 (br. s., 2H),
7.31-7.27 (m, 1H), 7.13 (d, J=8.0 Hz, 1H), 5.32 (d, J=7.2 Hz, 1H),
4.80 (s, 1H), 4.76 (d, J=6.0 Hz, 1H), 4.83-4.72 (m, 3H), 3.41 (s,
1H), 3.24 (s, 3H), 3.02-2.90 (m, 1H), 2.55 (s, 1H), 2.39-2.10 (m,
4H), 1.95-1.80 (m, 1H), 1.75-1.59 (m, 2H), 1.50 (br. s., 1H), 1.34
(s, 8H), 1.16-1.05 (m, 4H), 0.97 (d, J=7.0 Hz, 3H), 0.66 (d, J=6.8
Hz, 3H). MS (ESI): mass calcd. for
C.sub.31H.sub.42BF.sub.4NO.sub.11S 609.26, m/z found 608.3
[M-H].sup.-. HPLC: 99.9% (220 nm), 100% (254 nm). [0377] 51.
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-((E)-2-(5-m-
ethyl-1,3,4-oxadiazol-2-yl)vinyl)-3-oxodecahydro-4,9a-propanocyclopenta[8]-
annulen-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)o-
xy)acetate
##STR00150##
[0378] To a mixture of
(E)-3-((3aR,4R,5R,7S,8S,9R,9aS,12R)-5-(2-((7-fluoro-1-hydroxy-1,3-dihydro-
benzo[c][1,2]oxaborol-6-yl)oxy)acetoxy)-8-hydroxy-4,7,9,12-tetramethyl-3-o-
xodecahydro-4,9a-propanocyclopenta[8]annulen-7-yl)acrylic acid
(500.0 mg, 873.5 umol, 1.0 eq), HATU (365.3 mg, 960.8 umol, 1.1 eq)
and TEA (176.8 mg, 1.75 mmol, 242.15 uL, 2.00 eq) in DMF (10.00 mL)
was added acetohydrazide (129.4 mg, 1.8 mmol, 2.00 eq) in one
portion at 25.degree. C. The mixture was stirred at 25.degree. C.
for 1 hr. H.sub.2O (50 mL) was added the mixture, which was
acidified with aqueous HCl (2 M) till PH=5-6 to precipitate a white
solid. The reaction mixture was filtered and the cake was washed
with 10 mL of H.sub.2O, dried to give
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-((E)-3-(2-acetylhydrazinyl)-3-oxoprop-1-en-
-1-yl)-8-hydroxy-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopent-
a[8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6--
yl)oxy)acetate (500.0 mg, crude) as white solid.
[0379] To a mixture of
(3aR,4R,5R,7S,8S,9R,9aS,12R)-7-((E)-3-(2-acetylhydrazinyl)-3-oxoprop-1-en-
-1-yl)-8-hydroxy-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propanocyclopent-
a[8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6--
yl)oxy)acetate (500.0 mg, 795.6 umol, 1.0 eq) in DCM (10.0 mL) was
added TEA (161.0 mg, 1.6 mmol, 220.6 uL, 2.0 eq) and TosCl (151.7
mg, 795.6 umol, 1.0 eq) in one portion at 25.degree. C. The mixture
was stirred at 25.degree. C. for 20 hrs. H.sub.2O (30 mL) was added
the mixture, which was acidified with aqueous HCl (2 M) till pH=5-6
to precipitate a white solid. The aqueous layer was extracted with
EtOAc (50 mL.times.3). The combined organic layers were washed with
brine (10 mL) and dried over Na.sub.2SO.sub.4. After filtration via
filter paper, the organic layer was concentrated under reduced
pressure to provide crude product, which was purified by prep-HPLC
(column: Luna C18 100.times.30 mm, 5 .mu.m; liquid phase:
[A-TFA/H.sub.2O=0.075% v/v; BACN]B %: 33%-63%, 12 min]) and
(column: Luna C18 100.times.30 mm, 5 .mu.m; liquid phase:
[A-TFA/H.sub.2O=0.075% v/v; B-ACN]B %: 35%-65%, 12 min]). After
prep-HPLC purification, the eluent was concentrated to remove
organic solvent. The residual aqueous solution was lyophilized to
give
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-((E)-2-(5-m-
ethyl-1,3,4-oxadiazol-2-yl)vinyl)-3-oxodecahydro-4,9a-propanocyclopenta[8]-
annulen-5-yl
2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(20.0 mg, 28.8 umol, 3.6% yield, 87.9% purity) as white solid.
.sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 7.22 (t, J=8.0 Hz, 1H),
7.09 (d, J=8.0 Hz, 1H), 6.87 (d, J=16.4 Hz, 1H), 6.28 (d, J=16.4
Hz, 1H), 5.59 (d, J=8.0 Hz, 1H), 4.93-4.74 (m, 4H), 3.68 (d, J=5.6
Hz, 1H), 2.44 (s, 1H), 2.28-2.00 (m, 4H), 1.73-1.59 (m, 2H),
1.54-1.44 (m, 1H), 1.42-1.23 (m, 7H), 1.17-0.87 (m, 7H), 0.81 (d,
J=7.1 Hz, 3H), 0.63 (d, J=6.6 Hz, 3H). MS (ESI): mass calcd. for
C.sub.32H.sub.40BFN.sub.2O.sub.8 610.3, m/z found 609.3
[M-H].sup.-. HPLC: 87.9% (220 nm), 98.3% (254 nm). [0380] 52.
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-((E)-2-(3-m-
ethyl-1,2,4-oxadiazol-5-yl)vinyl)-3-oxodecahydro-4,9a-propanocyclopenta[8]-
annulen-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)o-
xy)acetate
##STR00151##
[0381] To a mixture of
(E)-3-((3aR,4R,5R,7S,8S,9R,9aS,12R)-5-(2-((7-fluoro-1-hydroxy-1,3-dihydro
benzo[c][1,2]oxaborol-6-yl)oxy)acetoxy)-8-hydroxy-4,7,9,12-tetramethyl-3--
oxodecahydro-4,9a-propanocyclopenta[8]annulen-7-yl)acrylic acid
(500.0 mg, 873.5 umol, 1.0 eq), HATU (365.3 mg, 960.8 umol, 1.1 eq)
and TEA (176.8 mg, 1.7 mmol, 242.2 uL, 2.0 eq) in DMF (5.0 mL) was
added N'-hydroxyacetamidine (129.4 mg, 1.7 mmol, 2.0 eq) in one
portion at 25.degree. C. The mixture was stirred at 25.degree. C.
for 2 hrs. H.sub.2O (50 mL) was added to the mixture, which was
acidified with aqueous HCl (2 M) till pH=5-6 to precipitate a white
solid. The reaction mixture was filtered and the filter cake was
washed with 20 mL of H.sub.2O, dried to give
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-7-((E)-3-((Z)-N'-hydroxyacetimidam-
ido)-3-oxoprop-1-en-1-yl)-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propano-
cyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]ox-
aborol-6-yl)oxy)acetate (550.0 mg, crude) as white solid.
[0382] To a mixture of
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-7-((E)-3-((Z)-N'-hydroxyacetimidam-
ido)-3-oxoprop-1-en-1-yl)-4,7,9,12-tetramethyl-3-oxodecahydro-4,9a-propano-
cyclopenta[8]annulen-5-yl2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]ox-
aborol-6-yl)oxy) acetate (500.0 mg, 795.6 umol, 1.0 eq) in THE (5.0
mL) was added TosCl (303.4 mg, 1.6 mmol, 2.0 eq) and pyridine
(314.6 mg, 4.0 mmol, 321.1 uL, 5.0 eq) in one portion at 25.degree.
C. The mixture was stirred at 25.degree. C. for 30 hrs. A new peak
was detected, and some the starting material remained. H.sub.2O (20
mL) was added to the mixture, which was acidified with aqueous HCl
(2 M) till pH=5-6 to precipitate a white solid. The aqueous layer
was extracted with EtOAc (20 mL.times.3). The combined organic
layers were washed with brine (10 mL) and dried over
Na.sub.2SO.sub.4. After filtration via filter paper, the organic
layer was concentrated under reduced pressure to provide a crude
product, which was purified by prep-HPLC (column: Luna C18
100.times.30 mm, 5 .mu.m; liquid phase: [A-TFA/H.sub.2O=0.075% v/v;
BACN]B %: 38%-68%, 12 min]). After prep-HPLC purification, the
eluent was concentrated to remove organic solvents. The residual
aqueous solution was lyophilized to give
(3aR,4R,5R,7S,8S,9R,9aS,12R)-8-hydroxy-4,7,9,12-tetramethyl-7-((E)-2-
-(3-methyl-1,2,4-oxadiazol-5-yl)vinyl)-3-oxodecahydro-4,9a-propanocyclopen-
ta[8]annulen-5-yl
2-((7-fluoro-1-hydroxy-1,3-dihydrobenzo[c][1,2]oxaborol-6-yl)oxy)acetate
(26.0 mg, 38.4 umol, 4.8% yield, 90.1% purity) as white solid.
.sup.1H NMR (DMSO-d.sub.6, 400 MHz) .delta. 7.24-7.14 (m, 2H),
7.10-7.02 (m, 1H), 6.32 (d, J=16.3 Hz, 1H), 5.56 (d, J=7.9 Hz, 1H),
4.92-4.83 (m, 2H), 4.82-4.73 (m, 2H), 3.69 (d, J=6.2 Hz, 1H), 2.53
(br. s., 4H), 2.43 (d, J=1.8 Hz, 4H), 2.29 (s, 2H), 2.27-2.04 (m,
3H), 1.75-1.59 (m, 1H), 1.39-1.21 (m, 4H), 1.14 (s, 2H), 1.07-0.97
(m, 1H), 0.96-0.84 (m, 1H), 0.80 (d, J=7.1 Hz, 3H), 0.71 (s, 1H),
0.63 (d, J=7.1 Hz, 3H). MS (ESI): mass calcd. for
C.sub.32H.sub.40BFN.sub.2O.sub.8 610.5, m/z found 609.3
[M-H].sup.-. HPLC: 90.1% (220 nm), 98.6% (254 nm).
Example 2
Antibacterial MIC Assays
[0383] All MIC testing of bacteria followed the Clinical and
Laboratory Standards Institute (CLSI) guidelines for antimicrobial
testing of aerobic bacteria (Methods for Dilution Antimicrobial
Susceptibility Tests for Bacteria that Grow Aerobically; Approved
Standard--Tenth Edition, M07-A10; Performance Standards for
Antimicrobial Susceptibility Testing; Twenty-fifth Informational
Supplement, M100-S25).
[0384] Briefly, the microbroth dilution MIC method was used to
quantitatively measure the in vitro antibacterial activity of a
compound against a given bacterial isolate. The following bacterial
strains were evaluated: Staphylococcus aureus, MRSA (ATCC 33591)
and Streptococcus pneumoniae (ATCC 49619). Bacteria were grown in
cation-adjusted Mueller-Hinton broth, with additions as required
per species growth requirements (e.g. 3% lysed horse blood for
fastidious organisms such as S. pneumoniae). A direct colony
suspension in saline was prepared from colonies on an overnight
agar plate to achieve a turbidity equivalent to 0.5 McFarland
standard, which was subsequently diluted into the assay plate to
achieve 5.times.10.sup.5 CFU/mL. Assays plates were prepared by
2-fold dilution of compound across the plate and included a
positive growth control. After incubation at 35.degree. C. for
16-20 hours, the MIC was determined as the lowest concentration of
compound that inhibits growth of the bacteria as detected by the
unaided eye.
Anti-Wolbachia High-Content Assay
[0385] C6/36 cells (ECACC #89051705, derived from Aedes albopictus
larvae) were infected with Wolbachia pipientis derived from the
supernatant of cultured A. albopictus Aa23 cells to create a stably
Wolbachia-infected cell line C6/36 (wAlbB). This cell line was
subpassaged 6-8 days prior to plating out at a density of 2000
viable cells per well in a 384-well CellCarrier plate suspended in
Liebovitz media supplemented with 20% fetal bovine serum, 2%
tryptose phosphate broth and 1% non-essential amino acids.
Compounds were dissolved and diluted in DMSO, and compound solution
was added to each well to provide a final DMSO concentration <1%
and a total volume of 100 .mu.L per well.
[0386] Following 7 days of sterile incubation at 26.degree. C.,
staining media containing SYTO 11 DNA dye was added to each well.
After 15 minutes, all media was removed from each well and fresh
media (no stain) was added. Imaging of each well was accomplished
using a Perkin Elmer Operetta high-content imaging system. Five
fields per well were imaged using a confocal 60.times. objective
with the Fluorescein filter (excitation filter: 460-490 nm;
emission filter: 500-550 nm). Images were analyzed using the Perkin
Elmer Harmony software to score each intact cell on the basis of
texture complexity of the cytoplasm. Full details can be found in:
Clare, R. H. etal, J. Biomol. Screening, 2015, 20, 64-49.
[0387] Compound sample wells were analyzed and normalized (along
with the positive controls) against the vehicle (untreated) control
to give a percentage reduction of Wolbachia-infected cells. Using
the cell number analysis, compounds with a host cell number
amounting to less than 50% of the vehicle control were classified
as toxic and retested at a reduced compound concentration.
Dose-response curves were generated with percentage reduction of
Wolbachia-infected cells versus compound concentration, using 5-10
compound serial dilutions. Data were analyzed and compound
EC.sub.50 is determined using a 4 parameter logistic nonlinear
regression model. EC.sub.50 is defined as the compound
concentration producing a 50% reduction of Wolbachia in the C6/36
cell line.
[0388] Antibacterial testing results for exemplary compounds of the
invention are provided below. Units for MIC are .mu.g/mL. Units for
EC50 are .mu.M. MIC of .ltoreq.0.25 is A, 0.5-2 is B, 4-32 is C,
and .gtoreq.64 is D.
TABLE-US-00001 MIC MIC EC50 Wolbachia Staphylococcus Streptococcus
pipientis in Compound aureus, MRSA pneumoniae C6/36 # (ATCC 33591)
(ATCC 49619) cell line 1. B C >1 2. C C >1 3. B B >1 4. B
B 0.283 5. B B 0.305 6. B B 0.392 7. C B 8. C B 9. C C 10. A B 11.
A B 12. A A 0.081 13. C D >1 14. B B 15. B B 16. C B 17. C B 18.
C B 19. A B 0.038 20. A B 0.101 21. A B 22. A B 23. A C >1 24. A
C 25. B C 26. A C 27. A B 0.148 28. D D >1 29. A C 30. B C 31. A
B 0.278 32. B C >1 33. B C 0.328 34. C C 0.474 35. C C 0.357 36.
B C 0.116 37. B C 0.372 38. B C 39. C C 40. C D 41. C C 42. C D 43.
A C >1 44. A C 0.197 45. B C 46. B C 47. B C >1 48. B C >1
49. C D >1 50. C C 51. B B 52. A A
[0389] It is understood that the examples and embodiments described
herein are for illustrative purposes only and that various
modifications or changes in light thereof will be suggested to
persons skilled in the art and are to be included within the spirit
and purview of this application and scope of the appended claims.
All publications, patents, and patent applications cited herein are
hereby incorporated by reference in their entirety for all
purposes.
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