U.S. patent application number 11/823776 was filed with the patent office on 2007-11-22 for diaminopyrroloquinazolines compounds as protein tyrosine phosphatase inhibitors.
Invention is credited to Steven Joseph Berthel, Adrian Wai-Hing Cheung, Kyungjin Kim, Kshitij Chhabilbhai Thakkar, Weiya Yun.
Application Number | 20070270445 11/823776 |
Document ID | / |
Family ID | 33457200 |
Filed Date | 2007-11-22 |
United States Patent
Application |
20070270445 |
Kind Code |
A1 |
Berthel; Steven Joseph ; et
al. |
November 22, 2007 |
Diaminopyrroloquinazolines compounds as protein tyrosine
phosphatase inhibitors
Abstract
The invention relates to
pyrimido[5,4-e][1,2,4]triazine-5,7-diamine compounds which are
useful for inhibiting protein tyrosine phosphatases, particularly
PTP1B, and are useful for lowering blood glucose concentrations in
mammals.
Inventors: |
Berthel; Steven Joseph;
(Mendham Township, NJ) ; Cheung; Adrian Wai-Hing;
(Glen Rock, NJ) ; Kim; Kyungjin; (Livingston,
NJ) ; Thakkar; Kshitij Chhabilbhai; (Nutley, NJ)
; Yun; Weiya; (Warren, NJ) |
Correspondence
Address: |
HOFFMANN-LA ROCHE INC.;PATENT LAW DEPARTMENT
340 KINGSLAND STREET
NUTLEY
NJ
07110
US
|
Family ID: |
33457200 |
Appl. No.: |
11/823776 |
Filed: |
June 27, 2007 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
10836507 |
Apr 30, 2004 |
7262297 |
|
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11823776 |
Jun 27, 2007 |
|
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60470803 |
May 15, 2003 |
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60563584 |
Apr 19, 2004 |
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Current U.S.
Class: |
514/267 ;
544/250 |
Current CPC
Class: |
A61P 5/50 20180101; A61P
3/10 20180101; A61P 43/00 20180101; A61P 3/08 20180101; C07D 487/04
20130101; A61P 3/00 20180101 |
Class at
Publication: |
514/267 ;
544/250 |
International
Class: |
A61K 31/519 20060101
A61K031/519; A61P 3/00 20060101 A61P003/00; C07D 487/04 20060101
C07D487/04 |
Claims
1. A compound of the formula: ##STR138## wherein {circle around
(P)} is a 5 or 6 membered heteroaromatic ring containing from 1 to
2 hetero atoms selected from the group consisting of oxygen,
sulfur, and nitrogen; R.sub.1 is selected from hydrogen and lower
alkyl; R.sub.2 is selected from the group consisting of hydrogen,
##STR139## R.sub.3 and R.sub.4 are independently selected from the
group consisting of hydrogen, lower alkyl, lower alkenyl, lower
alkoxy, hydroxy lower alkyl, perfluoroloweralklyl, nitro, halo,
lower alkanoyl, --N R.sub.5R.sub.6, R.sub.7S--, ##STR140## phenyl,
hydroxy, perfluoroloweralkoxy, and phenoxy, or R.sub.3 and R.sub.4
when present on adjacent carbon atoms on the heteroaromatic ring
can be taken together to form a lower alkylene bridge or taken
together with their adjacent carbon atoms to form an aromatic ring
system fused to the heteroaromatic ring, said aromatic ring system
containing one or two aromatic rings with one of said rings being
either an aromatic or heteroaromatic ring; R.sub.5 and R.sub.6 are
selected from hydrogen and lower alkyl; R.sub.2 is selected from
the group consisting of hydrogen, benzyl, phenyl and lower alkyl;
R.sub.7 is lower alkyl; R.sub.13 is selected from the group
consisting of hydrogen, lower alkyl, benzyl and phenyl; R.sub.10,
R.sub.11 and R.sub.12 are independently selected from hydrogen and
lower alkyl; and m, n, o and v are independent integers selected
from 0 to 4, or pharmaceutically acceptable salts thereof,
2. The compound of claim 1 wherein {circle around (P)} is a
heteroaromatic ring containing sulfur as the only hetero atom.
3. The compound of claim 2 wherein R.sub.3 and R.sub.4 are
independently selected from hydrogen, halogen and lower alkyl.
4. The compound of claim 3 wherein said compound is
7-methanesulfonyl-6-thiophen-2-yl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamin-
e trifluoro-acetic acid salt.
5. The compound of claim 3 wherein said compound is
7-methyl-6-thiophen-2-yl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine.
6. The compound of claim 3 wherein said compound is
6-(5-chloro-thiophen-2-yl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt.
7. The compound of claim 2 wherein R.sub.3 and R.sub.4 is selected
from hydrogen and ##STR141## R.sub.12 is selected from hydrogen and
lower alkyl; and R.sub.3 and R.sub.4 are other than hydrogen.
8. The compound of claim 7 wherein said compound is
1-[5-(1,3-diamino-7H-pyrrolo[3,2-f]quinazolin-6-yl)-thiophen-2-yl]-ethano-
ne trifluoro-acetic acid salt.
9. The compound of claim 7 wherein said compound is
1-[5-(1,3-diamino-7-methyl-7H-pyrrolo[3,2-f]quinazolin-6-yl)-thiophen-2-y-
l]-ethanone trifluoro-acetic acid salt.
10. The compound of claim 1 wherein R.sub.3 and R.sub.4 are
attached to the hetero atom ring on adjacent carbon atoms and taken
together with their attached carbon atoms a fused phenyl ring.
11. The compound of claim 10 wherein said compound is
6-benzo[b]thiophen-2-yl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt.
12. The compound of claim 10 wherein said compound is
6-benzo[b]thiophen-2-yl-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt.
13. The compound of claim 7 wherein said compound is
6-benzofuran-2-yl-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine.
14. The compound of claim 1 wherein {circle around (P)} is a
heteroaromatic ring containing an oxygen atom as the only hetero
atom.
15. The compound of claim 14 wherein said compound is
6-furan-2-yl-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt.
16. The compound of claim 14 wherein said compound is
6-benzofuran-2-yl-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
17. The compound of claim 1 wherein {circle around (P)} is a
heteroaromatic ring containing a nitrogen hetero atom.
18. The compound of claim 17 wherein said compound is
6-(3,5-dimethyl-isoxazol-4-yl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3--
diamine trifluoro-acetic acid salt.
19. A pharmaceutical composition comprising one or more compounds
of the formula ##STR142## and one or more pharamceutically
acceptable excipients wherein {circle around (P)} is a 5 or 6
membered heteroaromatic ring containing from 1 to 2 hetero atoms
selected from the group consisting of oxygen, sulfur, and nitrogen;
R.sub.1 is selected from hydrogen and lower alkyl; R.sub.2 is
selected from the group consisting of hydrogen, ##STR143## R.sub.3
and R.sub.4 are independently selected from the group consisting of
hydrogen, lower alkyl, lower alkenyl, lower alkoxy, hydroxy lower
alky, perfluoroloweralklyl, nitro, halo, lower alkanoyl, --N
R.sub.5R.sub.6, R.sub.7S--, ##STR144## phenyl, hydroxy,
perfluoroloweralkoxy, and phenoxy, or R.sub.3 and R.sub.4 when
present on adjacent carbon atoms on the heteroaromatic ring can be
taken together with their adjacent carbon atoms to form a lower
alkylenedioxy bridge or an aromatic ring system fused to the phenyl
ring, said aromatic ring system containing one or two aromatic
rings with one of said rings being either an aromatic or
heteroaromatic ring; R.sub.5 and R.sub.6 are selected from hydrogen
and lower alkyl; R.sub.2 is selected from the group consisting of
hydrogen, benzyl, phenyl and lower alkyl; R.sub.7 is lower alkyl;
R.sub.13 is selected from the group consisting of hydrogen, lower
alkyl, benzyl and phenyl; R.sub.10, R.sub.11 and R.sub.12 are
independently selected from hydrogen and lower alkyl; and m, n, o
and v are independent integers selected from 0 to 4 or
pharmaceutically acceptable salts thereof.
20. A method of treating a disease based on high blood glucose
concentration comprising administering to a patient in need of such
treatment a therapeutically effective amount of at least one
compound of the formula: ##STR145## wherein, {circle around (P)} is
a 5 or 6 membered heteroaromatic ring containing from 1 to 2 hetero
atoms selected from the group consisting of oxygen, sulfur, and
nitrogen; R.sub.1 is selected from hydrogen and lower alkyl;
R.sub.2 is selected from the group consisting of hydrogen,
##STR146## R.sub.3 and R.sub.4 are independently selected from the
group consisting of hydrogen, lower alkyl, lower alkenyl, lower
alkoxy, hydroxy lower alkyl, perfluoroloweralklyl, nitro, halo,
lower alkanoyl, --N R.sub.5R.sup.6, R.sub.7S--, ##STR147## phenyl,
hydroxy, perfluoroloweralkoxy, and phenoxy, or R.sub.3 and R.sub.4
when present on adjacent carbon atoms on the heteroaromatic ring
can be taken together with their adjacent carbon atoms to form a
lower alkylenedioxy bridge or an aromatic ring system fused to the
phenyl ring, said aromatic ring system containing one or two
aromatic rings with one of said rings being either an aromatic or
heteroaromatic ring; R.sub.5 and R.sub.6 are selected from hydrogen
and lower alkyl; R.sub.2 is selected from the group consisting of
hydrogen, benzyl, phenyl and lower alkyl; R.sub.7 is lower alkyl;
R.sub.13 is selected from the group consisting of hydrogen, lower
alkyl, benzyl and phenyl; R.sub.10, R.sub.11 and R.sub.12 are
independently selected from hydrogen and lower alkyl; and m, n, o
and v are independent integers selected from 0 to 4 or
pharmaceutically acceptable salts thereof.
Description
PRIORITY TO RELATED APPLICATIONS
[0001] This application is a division of U.S. application Ser. No.
10/836,507 filed Apr. 30, 2004, which is now pending. This
application claims priority under 35 U.S.C. .sctn.119(e) of
provisional application(s) Ser. No. 60/470,803, filed May 15, 2003
and Ser. No. 60/563,584, filed Apr. 19, 2004.
FIELD OF THE INVENTION
[0002] The invention relates to diaminopyrroloquinazolines
compounds useful for inhibiting protein tyrosine phosphatases,
particularly PTP1B, and are useful for lowering blood glucose
concentrations in mammals.
BACKGROUND OF THE INVENTION
[0003] Protein tyrosine phosphatases (PTPases) are key enzymes in
processes that regulate cell growth and differentiation. The
inhibition of these enzymes can play a role in the modulation of
multiple signaling pathways in which tyrosine phosphorylation
dephosphorylation plays a role. PTP1B is a particular protein
tyrosine phosphatases that is often used as a prototypical member
of that class of enzymes.
[0004] PTPase inhibitors are recognized as potential therapeutic
agents for the treatment of diabetes. See, e.g. Moeller et al.,
3(5):527-40, Current Opinion in Drug Discovery and Development,
2000; or Zhang, Zhong-Yin, 5:416-23, Current Opinion in Chemical
Biology, 2001. The utility of PTPase inhibitors as therapeutic
agents has been a topic of discussion in several review articles
including, for example, Expert Opin Investig Drugs, 12(2):223-33,
February 2003.
SUMMARY OF THE INVENTION
[0005] It has been discovered that compounds of the formula:
##STR1## wherein [0006] R.sub.1 is selected from hydrogen and lower
alkyl; [0007] R.sub.2 is selected from the group consisting of
hydrogen, lower alkyl, ##STR2## [0008] R.sub.3 and R.sub.4 are
independently selected from the group consisting of hydrogen, lower
alkyl, lower alkenyl, lower alkoxy, hydroxy lower alkyl,
perfluoroloweralklyl, nitro, halo, lower alkanoyl, --N
R.sub.5R.sub.6, R.sub.7S--, ##STR3## [0009] phenyl, hydroxy,
perfluoroloweralkoxy, and phenoxy, or [0010] R.sub.3 and R.sub.4
when present on adjacent carbon atoms on the phenyl ring can be
taken together with their adjacent carbon atoms to form a lower
alkylenedioxy bridge or an aromatic ring system fused to the phenyl
ring, said aromatic ring system containing one or two aromatic
rings with one of said rings being either an aromatic or
heteroaromatic ring; [0011] R.sub.5 and R.sub.6 are independently
selected from hydrogen and lower alkyl; [0012] R.sub.12 is selected
from the group consisting of hydrogen, benzyl, phenyl and lower
alkyl; [0013] R.sub.7 is lower alkyl; [0014] R.sub.13 is selected
from the group consisting of hydrogen, lower alkyl, benzyl and
phenyl; [0015] R.sub.10, R.sub.11 and R.sub.12 are independently
selected from hydrogen and lower alkyl; and [0016] m, n, o and v
are independent integers selected from 0 to 4, or pharmaceutically
acceptable salts thereof, [0017] inhibit protein tyrosine
phosphatases, particularly PTP1B and are therefore useful for
lowering blood glucose concentrations in mammals.
[0018] In another embodiment, it has also been discovered that
compounds of the formula: ##STR4##
[0019] wherein [0020] {circle around (P)} is a 5 or 6 membered
heteroaromatic ring containing from 1 to 2 hetero atoms selected
from the group consisting of oxygen, sulfur, and nitrogen; [0021]
R.sub.1 is selected from hydrogen and lower alkyl; [0022] R.sub.2
is selected from the group consisting of hydrogen, lower alkyl,
##STR5## [0023] R.sub.3 and R.sub.4 are independently selected from
the group consisting of hydrogen, lower alkyl, lower alkenyl, lower
alkoxy, hydroxy lower alkyl, perfluoroloweralklyl, nitro, halo,
lower alkanoyl, --N R.sub.5R.sub.6, R.sub.7S--, ##STR6## [0024]
phenyl, hydroxy, perfluoroloweralkoxy, and phenoxy, or [0025]
R.sub.3 and R.sub.4 when present on adjacent carbon atoms on the
heteroaromatic ring can be taken together with their adjacent
carbon atoms to form a lower alkylenedioxy bridge or an aromatic
ring system fused to the phenyl ring, said aromatic ring system
containing one or two aromatic rings with one of said rings being
either an aromatic or heteroaromatic ring; [0026] R.sub.5 and
R.sub.6 are independently selected from hydrogen and lower alkyl;
[0027] R.sub.2 is selected from the group consisting of hydrogen,
benzyl, phenyl and lower alkyl; [0028] R.sub.7 is lower alkyl;
[0029] R.sub.13 is selected from the group consisting of hydrogen,
lower alkyl, benzyl and phenyl; [0030] R.sub.10, R.sub.11 and
R.sub.12 are independently selected from hydrogen and lower alkyl;
and [0031] m, n, o and v are independent integers selected from 0
to 4, or pharmaceutically acceptable salts thereof, inhibit protein
tyrosine phosphatases, particularly PTP1B and are therefore useful
for lowering blood glucose concentrations in mammals.
DETAILED DESCRIPTION OF THE INVENTION
[0032] The present invention comprises compounds of the formula:
##STR7## wherein [0033] R.sub.1 is selected from hydrogen and lower
alkyl; [0034] R.sub.2 is selected from the group consisting of
hydrogen, lower alkyl, ##STR8## [0035] R.sub.3 and R.sub.4 are
independently selected from hydrogen, lower alkyl, lower alkenyl,
lower alkoxy, hydroxy lower alkyl, perfluoroloweralklyl, nitro,
halo, lower alkanoyl, --N R.sub.5R.sub.6, R.sub.7S--, ##STR9##
[0036] phenyl, hydroxy, perfluoroloweralkoxy, and phenoxy, or
[0037] R.sub.3 and R.sub.4 when present on adjacent carbon atoms on
the phenyl ring can be taken together with their adjacent carbon
atoms to form a lower alkylenedioxy bridge or an aromatic ring
system fused to the phenyl ring, said aromatic ring system
containing one or two aromatic rings with one of said rings being
either an aromatic or heteroaromatic ring; [0038] R.sub.5 and
R.sub.6 are independently selected from hydrogen and lower alkyl;
[0039] R.sub.12 is selected from the group consisting of hydrogen,
benzyl, phenyl and lower alkyl; [0040] R.sub.7 is lower alkyl;
[0041] R.sub.13 is selected from the group consisting of hydrogen,
lower alkyl, benzyl and phenyl; [0042] R.sub.10, R.sub.11 and
R.sub.12 are independently selected from hydrogen and lower alkyl;
and [0043] m, n, o and v are independent integers selected from 0
to 4, or pharmaceutically acceptable salts thereof, inhibit protein
tyrosine phosphatases, particularly PTP1B and are therefore useful
for lowering blood glucose concentrations in mammals.
[0044] Another embodiment of the compounds of this invention
comprises compounds of the formula: ##STR10## wherein [0045]
{circle around (P)} is a 5 or 6 membered heteroaromatic ring
containing from 1 to 2 hetero atoms selected from the group
consisting of oxygen, sulfur, and nitrogen; [0046] R.sub.1 is
selected from hydrogen and lower alkyl; [0047] R.sub.2 is selected
from the group consisting of hydrogen, lower alkyl, ##STR11##
[0048] R.sub.3 and R.sub.4 are independently selected from the
group consisting of hydrogen, lower alkyl, lower alkenyl, lower
alkoxy, hydroxy lower alkyl, perfluoroloweralklyl, nitro, halo,
lower alkanoyl, --N R.sub.5R.sub.6, R.sub.7S--, ##STR12## [0049]
phenyl, hydroxy, perfluoroloweralkoxy, and phenoxy, or [0050]
R.sub.3 and R.sub.4 when present on adjacent carbon atoms on the
heteroaromatic ring can be taken together with their adjacent
carbon atoms to form a lower alkylenedioxy bridge or an aromatic
ring system fused to the phenyl ring, said aromatic ring system
containing one or two aromatic rings with one of said rings being
either an aromatic or heteroaromatic ring; [0051] R.sub.5 and
R.sub.6 are independently selected from hydrogen and lower alkyl;
[0052] R.sub.2 is selected from the group consisting of hydrogen,
benzyl, phenyl and lower alkyl; [0053] R.sub.7 is lower alkyl;
[0054] R.sub.13 is selected from the group consisting of hydrogen,
lower alkyl, benzyl and phenyl; [0055] R.sub.10, R.sub.11 and
R.sub.12 are independently selected from hydrogen and lower alkyl;
and [0056] m, n, o and v are independent integers selected from 0
to 4, or pharmaceutically acceptable salts thereof, inhibit protein
tyrosine phosphatases, particularly PTP1B and are therefore useful
for lowering blood glucose concentrations in mammals.
[0057] As used in the specification, the term "lower alkyl", alone
or in combination, means a straight-chain or branched-chain alkyl
group containing from one to six carbon atoms, such as methyl,
ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl,
tert-butyl, n-pentyl, n-hexyl and the like.
[0058] The term "cycloalkyl" means an unsubstituted or substituted
3- to 7-membered saturated carbocyclic ring.
[0059] The term "lower alkoxy" means a straight-chain or
branched-chain alkoxy group containing from one to six carbon
atoms, such as methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy,
tert-butoxy and the like.
[0060] The term "heteroaromatic" means a mono-cyclic heteroaromatic
ring or a fused ring system containing one or more hetero atoms in
the ring system such as nitrogen atom, oxygen atom and sulphur atom
within the ring or ring system. Examples of "heteroaryl group" are
pyridyl group, thienyl group and furyl.
[0061] The term "aryl" means a mono- or bicyclic aromatic group,
such as phenyl or naphthyl, which is unsubstituted or substituted
by conventional substituent groups.
[0062] The term "lower alkylenedioxy" denotes a divalent saturated
hydrocarbon moiety containing from one to six carbon atoms having
terminal oxygens which are placed at the end of the lower alkylene
chain and connect to the rest of the molecule. The preferred lower
alkylenedioxy moieties are 1,2-ethylene dioxy, methylene dioxy,
1,3-propylene dioxy. Generally, the preferred lower alkylene dioxy
moieties are formed in a straight chain.
[0063] The term "pharmaceutically acceptable salts" refers to
conventional acid-addition salts or base-addition salts that retain
the biological effectiveness and properties of the compounds of
formulas I, II, III and IV and are formed from suitable non-toxic
organic or inorganic acids, or organic or inorganic bases. Sample
acid-addition salts include those derived from inorganic acids such
as hydrochloric acid, hydrobromic acid, hydroiodic acid, sulfuric
acid, sulfamic acid, phosphoric acid and nitric acid, and those
derived from organic acids such as p-toluenesulfonic acid,
salicylic acid, methanesulfonic acid, oxalic acid, succinic acid,
citric acid, malic acid, lactic acid, fumaric acid, and the like.
Sample base-addition salts include those derived from ammonium,
potassium, sodium and, quaternary ammonium hydroxides, such as for
example, tetramethylammonium hydroxide. The chemical modification
of a pharmaceutical compound (i.e., drug) into a salt is a
technique well known to pharmaceutical chemists to obtain improved
physical and chemical stability, hygroscopicity, flowability and
solubility of compounds. See, e.g., H. Ansel et al., Pharmaceutical
Dosage Forms and Drug Delivery Systems (6th Ed. 1995) at pp. 196
and 1456-1457.
[0064] The preferred compounds of the Compounds of Formula I-A and
I-B above are those compounds where R.sub.1 is hydrogen.
Particularly preferred among those classes of compounds where
R.sub.1 is hydrogen are those compounds where R.sub.2 is hydrogen
or lower alkyl.
[0065] There are many different embodiments of the compounds of
formula I-A. The main embodiments of the compounds of formula I-A
are first, those compounds where R.sub.3 and R.sub.4 are present on
the phenyl ring on the compound of formula I-A on adjacent carbon
atoms and taken together form a lower alkylene dioxy bridge. The
second major embodiment are those compounds of formula I-A where
R.sub.3 and R.sub.4 are present on adjacent carbon atoms on the
phenyl ring and are taken together with their adjacent carbon atoms
to form an aromatic ring system fused to the phenyl ring. The third
major embodiment are those compounds where R.sub.3 and R.sub.4 are
individual, connected to the phenyl ring.
[0066] In the first embodiment where R.sub.3 and R.sub.4 form a
lower alkylenedioxy bridge, these bridges preferably contain from
one to three carbon atoms. In a preferred class of this embodiment,
R.sub.2is hydrogen or lower alkyl and R.sub.1 is hydrogen or lower
alkyl, preferably hydrogen.
[0067] The second major embodiment of the compounds of formula I-A
are those compounds where R.sub.3 and R.sub.4 are substituted on
adjacent carbon atoms and taken together with their attached carbon
atoms form a fused aromatic ring system containing from 1 to 3
fused rings fused to the phenyl ring on the compound of formula
I-A. One class of compounds in this embodiment are those compounds
where the fused aromatic ring system, fused to the phenyl ring on
the compound of formula I-A, can contain one hetero aromatic ring
and/or one hetero aromatic and/or one aromatic ring. In the
embodiment where R.sub.3 and R.sub.4 form a fused aromatic ring
system, R.sub.1 is preferably hydrogen and R.sub.2 is preferably
hydrogen or lower alkyl. In this second major embodiment of the
compounds of formula I-A, another class of compounds are those
compounds where R.sub.3 and R.sub.4 when taken together with their
attached carbon atoms form a single fused heteroaromatic ring or an
aromatic ring such as phenyl. In this embodiment R.sub.1 and
R.sub.2 are preferably hydrogen or lower alkyl. In this second
major embodiment of the compounds of formula I-A, another class of
compounds are those compounds where R.sub.3 and R.sub.4 when taken
together with their attached carbon atoms form a two membered fused
ring system which is fused to the phenyl group on the compound of
formula I. These two membered ring systems can be both aromatic
rings or one hetero aromatic ring and one aromatic ring.
[0068] In the third major embodiment, R.sub.3 and R.sub.4 are
independent groups separately attached to the phenyl moiety in the
compound of formula I-A. One of the compounds within this
embodiment include compounds where R.sub.1 and R.sub.2 are
independently hydrogen or lower alkyl and R.sub.3 and R.sub.4 are
independently hydrogen, lower alkyl or lower alkenyl. In this
preferred group of compounds, lower alkenyl denotes a monovalent
aliphatic hydrocarbon substituent containing from two to six carbon
atoms and having an unsubstituted double bond within its structure.
The preferred group of compounds where R.sub.4 is lower alkenyl are
compounds where R.sub.3 is hydrogen and R.sub.1 and R.sub.2 are
independently hydrogen or lower alkyl.
[0069] Another class of compounds within the compounds of formula
I-A where R.sub.3 and R.sub.4 are independent substituents are
those compounds where R.sub.3 and R.sub.4 are individually
hydrogen, halogen, trifluoroloweralkyl, preferably trifluoromethyl,
and trifluoroloweralkoxy, preferably trifluoromethoxy, with one of
R.sub.3 and R.sub.4 being other than hydrogen. Within this class of
compounds are those compounds where R.sub.1 and R.sub.2 are either
hydrogen or lower alkyl.
[0070] Another class of compounds within the embodiment of R.sub.3
and R.sub.4being individual separate substituents are those
compounds where R.sub.3 is hydrogen or halogen and R.sub.4 is
halogen, nitro, lower alkoxy, phenoxy, hydroxy or hydroxyalkyl.
Among this class of compounds, compounds where R.sub.1 and R.sub.2
are hydrogen or lower alkyl are preferred. In another class of
compounds within this embodiment, where R.sub.3 is halogen or
hydrogen, another class of compounds are those where R.sub.4 is:
##STR13## [0071] v is an integer from 0 to 4; [0072] R.sub.12 is
hydrogen or lower alkyl. In this embodiment, R.sub.4 can be either
an aldehyde, where R.sub.12 is H or a ketone where R.sub.12 is
lower alkyl. Also in this regard, R.sub.3 and R.sub.4 can form one
or two lower carboxylic acid groups.
[0073] In accordance with another embodiment of the compound of
formula I-A where R.sub.3 and R.sub.4 are independent substituents,
there are those compounds where R.sub.1 and R.sub.2 are
independently hydrogen or lower alkyl;R.sub.3 and R.sub.4 are
hydrogen, R.sub.7S--, R.sub.5R.sub.6N--, or ##STR14## [0074]
R.sub.5 and R.sub.6 are independently hydrogen or lower alkyl;
[0075] R.sub.7is lower alkyl; and [0076] one of R.sub.3 and R.sub.4
is other than hydrogen.
[0077] Furthermore, in accordance with the embodiment of this
invention where R.sub.3 and R.sub.4 in the compound of formula I-A
are independent substituents are those class of compounds where
R.sub.2 is ##STR15## [0078] R.sub.13 is hydrogen, phenyl, benzyl or
lower alkyl; and [0079] m and n is an integer from 0 to 4. In this
case R.sub.1 is generally hydrogen or lower alkyl, preferably
hydrogen. In addition, R.sub.3 and R.sub.4 can be halogen or
trifluoroalkyl, preferably trifluoromethyl with one of R.sub.3 and
R.sub.4 being halogen or hydrogen.
[0080] In another class of compounds where R.sub.3 and R.sub.4 are
separate independent substituents are those compounds where R.sub.2
is ##STR16## [0081] R.sub.10 and R.sub.11 are independently
hydrogen or lower alkyl. In this group of compounds, R1 is hydrogen
or lower alkyl, preferably hydrogen. Also, with respect to this
class of compounds, R.sub.3 and R.sub.4 are preferably hydrogen or
lower alkoxy.
[0082] The compound of formula I-B contains various different
embodiments in the same manner as the compound of formula I-A. The
first major embodiment are those compounds where R.sub.3 and
R.sub.4 taken together form a lower alkylene dioxy bridge. The
second are those compounds where R.sub.3 and R.sub.4taken together
with their adjacent carbon atoms to form an aromatic ring system
which contains one or two aromatic or heteroaromatic rings fused to
the heteroaromatic ring {circle around (P)} in the compound of
formula I-B. On the other hand, in accordance with a third
embodiment of this invention, the compound of R.sub.3 and R.sub.4
on the compound of formula I-B can be independent, individual
substituents. The embodiments formed in this manner are the same as
set forth with regard to compounds I-A.
[0083] In addition, since the compound of formula I-B contains
within its structure a heteroaromatic ring, this heteroaromatic
ring can contain sulfur, oxygen or nitrogen as the only hetero
atom. On the other hand, this structure can contain two hetero
atoms with each being the same or each being a different hetero
atom such as oxygen or nitrogen. One such embodiment of those
compounds, where the hetero aromatic ring contains sulfur as the
only hetero atom. In this embodiment, the class of compounds where
R.sub.3 and R.sub.4 are independently halogen or lower alkyl are
preferred. In addition, those class of compounds where R.sub.3 and
R.sub.4 are independently hydrogen, halogen or lower alkyl and
R.sub.1 and R.sub.2 are hydrogen and lower alkyl are especially
preferred.
[0084] In addition, with respect to those compounds of formula I-B
where the hetero aromatic ring in this compound contains the sulfur
atom as the only hetero atom in its ring, the class of compounds
where R.sub.3 and R.sub.4 is hydrogen, or ##STR17## [0085] R.sub.12
is hydrogen or lower alkyl; and [0086] R.sub.3 and R.sub.4 is other
than hydrogen are preferred. In this embodiment, those compounds
where R.sub.1 and R.sub.2 are hydrogen and lower alkyl are
especially preferred.
[0087] As indicated hereinabove, R.sub.3 and R.sub.4 which are
present when attached on adjacent carbon atoms on the hetero
aromatic ring can be taken together with their attached carbon
atoms to form a fused ring system. This ring system can be either a
hetero aromatic ring or an aromatic ring. The preferred fused
aromatic ring is a phenyl ring.
[0088] This invention is also directed to a pharmaceutical
composition comprising one or more compounds of formulas I-A and
I-B.
[0089] Moreover, this invention is directed to a method of treating
a disease based on high blood glucose concentration comprising
administering to a patient in need of such treatment a
therapeutically effective amount of at least one compound of the
formulas I-A and I-B.
[0090] The compounds of the invention can exist as stereoisomers
and diastereomers, all of which are encompassed within the scope of
the present invention.
[0091] The compounds of the invention inhibit PTP1B in vitro and
have been shown to lower blood glucose levels in vivo. Thus, the
compounds of the present invention would be useful for the
treatment of diabetes.
[0092] The compounds of the invention can be administered orally,
rectally, or parentally, e.g., intravenously, intramuscularly,
subcutaneously, intrathecally or transdermally; or sublingually, or
as opthalmalogical preparations. Capsules, tablets, suspensions or
solutions for oral administration, suppositories, injection
solutions, eye drops, salves or spray solutions are examples of
administration forms.
[0093] Intravenous, intramuscular, oral or inhalation
administration are preferred forms of use. The dosages in which the
compounds of the invention are administered in effective amount
depend on the nature of the specific active ingredient, the age and
requirements of the patient and the mode of administration. Dosages
may be determined by any conventional means, e.g., by dose-limiting
clinical trials. In general, dosages of about 0.1 to 100 mg/kg body
weight per day are preferred, with dosages of 1-25 mg/kg per day
being particularly preferred.
[0094] The invention further comprises pharmaceutical compositions
that contain a pharmaceutically effective amount of a compound of
the invention and a pharmaceutically acceptable carrier. Such
compositions may be formulated by any conventional means. Tablets
or granulates can contain a series of binders, fillers, carriers or
diluents. Liquid compositions can be, for example, in the form of a
sterile water-miscible solution. Capsules can contain a filler or
thickener in addition to the active ingredient. Furthermore,
flavor-improving additives as well as substances usually used as
preserving, stabilizing, moisture-retaining and emulsifying agents
as well as salts for varying the osmotic pressure, buffers and
other additives can also be present.
[0095] The previously mentioned carrier materials and diluents can
comprise any conventional pharmaceutically acceptable organic or
inorganic substances, e.g., water, gelatine, lactose, starch,
magnesium stearate, talc, gum arabic, polyalkylene glycols and the
like.
[0096] Oral unit dosage forms, such as tablets and capsules,
preferably contain from 25 mg to 1000 mg of a compound of the
invention. The compounds of the invention may be prepared by any
conventional means.
[0097] In accordance with this invention, the compounds herein as
well as their pharmaceutically acceptable salts are useful in the
control or prevention of illnesses associated with high blood
glucose concentration. A preferred indication associated with the
present invention is that associated with diabetes.
[0098] The dosage can vary within wide limits and will, of course,
have to be adjusted to the individual requirements in each
particular case. In the case of oral administration, the dosage for
adults may vary from about 0.01 mg to about 1000 mg per day of a
compound of formula I-A and I-B or of the corresponding amount of a
pharmaceutically acceptable salt thereof. The daily dosage may be
administered as single dose or in divided doses, and in addition,
the upper limit can also be exceeded when this is found to be
indicated.
[0099] A particular method is described in the following Schemes 1
and 2. The examples following each of the schemes provide a
detailed description of the schematic methods. In the following
reaction schemes ##STR18## designates a phenyl ring or {circle
around (P)} which is a heteroaromatic ring. In the following
schemes, R.sub.8 and R.sub.9 are the same as R.sub.3 and R.sub.4.
##STR19##
[0100] Compound II: A mixture of silver sulfate (100 g, 0.32 mol)
and iodine (82 g, 0.32 mol) in N,N-dimethylformamide (700 mL) and
ethanol (1400 mL) was treated with 5-nitro-2,3-dihydro-1H-indole I
(48 g, 0.29 mol). The resulting mixture was stirred at 25.degree.
C. for 1.5 h, filtered and the filter pad washed with ethyl
acetate. The filtrate was concentrated in vacuo to a volume of
approximately 500 mL. This solution was treated with a 1.0N aqueous
sodium thiosulfate solution (100 mL) and a saturated aqueous sodium
chloride solution (400 mL). The resulting precipitate was collected
by filtration, washed with water and petroleum ether, and dried in
vacuo to afford 7-iodo-5-nitro-2,3-dihydro-1H-indole II (83.9 g,
98.9%) as a white solid: .sup.1H NMR (DMSO-d.sub.6, 300 MHz)
.delta. 8.18 (d, J=2.20 Hz, 1H), 7.80 (d, J=1.46 Hz, 1H), 7.03
(broad s, 1H), 3.65 (t, J=8.97 Hz, 2H), 3.17 (t, J=8.60 Hz,
2H).
[0101] Compound III: A solution of
7-iodo-5-nitro-2,3-dihydro-1H-indole II (15 g, 51.7 mmol) in
ethanol (1200 mL) and isopropanol (20 mL) at 25.degree. C. was
treated with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (13.6 g,
59.9 mmol). The resulting solution was warmed to 65.degree. C. and
air was bubbled through for 1 h. An additional 0.57 equivalents of
2,3-dichloro-5,6-dicyano-1,4-benzoquinone (6.8 g, 29.9 mmol) was
added and the reaction was stirred at 65.degree. C. for another 2 h
before being concentrated in vacuo. Flash chromatography (Merck
Silica gel 60, 230-400 mesh, 90/10 toluene/ethyl acetate) afforded
7-iodo-5-nitro-1H-indole III (13.07 g, 79%) as a yellow solid:
.sup.1H NMR (DMSO-d.sub.6, 300 MHz) .delta. 11.82 (broad s, 1H),
8.59 (d, J=1.83 Hz, 1H), 8.30 (d, J=1.83 Hz, 1H), 7.61 (t, J=2.93
Hz, 1H), 6.90 (dd, J.sub.1=1.83 Hz, J.sub.2=3.30 Hz, 1H).
[0102] Compound IV: A solution of 7-iodo-5-nitro-1H-indole III (20
g, 69.4 mmol) in methanol (650 mL) at 25.degree. C. was treated
with a solution of ammonium chloride (26.1 g, 485.8 mmol) in water
(550 mL) and iron powder (13.6 g, 242.9 mmol). The mixture was
heated to 100.degree. C. under a nitrogen atmosphere for 5 h. The
resulting mixture was filtered through a pad of celite and the
celite pad washed with hot methanol. The filtrate was concentrated
in vacuo and the residue was partitioned between methylene chloride
and water and separated. The pH of the aqueous layer was adjusted
to pH=10 with ammonium hydroxide and extracted with methylene
chloride. The combined organic layers were dried over sodium
sulfate, filtered, and concentrated in vacuo to a volume of 250 mL.
This solution was treated with a 4.0M aqueous hydrochloric acid
solution in dioxane and stirred at 25.degree. C. for 2 h. The
precipitate was collected by filtration and washed with methylene
chloride and petroleum ether to afford 7-iodo-1H-indol-5-ylamine
hydrochloride IV (24.7 g, quant.) as a gray solid: .sup.1H NMR
(DMSO-d.sub.6, 300 MHz) .delta. 11.34 (broad s, 1H), 9.93 (broad s,
2H), 7.56 (d, J=1.46 Hz, 1H), 7.48 (t, J=2.74 Hz, 1H), 7.44 (d,
J=1.83 Hz, 1H), 6.68 (dd, J.sub.1=1.83 Hz, J.sub.2=2.93 Hz,
1H).
[0103] Compound V: A solution of 7-iodo-1H-indol-5-ylamine
hydrochloride IV (24.6 g, 83.7 mmol) in N,N-dimethylformamide (400
mL) at 25.degree. C. was treated with sodium dicyanamide (18.6 g,
209 mmol). The reaction mixture was warmed to 50.degree. C. for 2
h, concentrated in vacuo, and the residue treated with water (500
mL). The resulting mixture was allowed to stand at 25.degree. C.
for 2.5 h during which time a yellow precipitate formed. The
precipitate was collected by filtration and washed with water to
afford N''-cyano-N-(7-iodo-1H-indol-5-yl)guanidine V (22.59 g, 83%)
as a light yellow solid: .sup.1H NMR (DMSO-d.sub.6, 300 MHz)
.delta. 11.02 (broad s, 1H), 8.89 (broad s, 1H), 7.46 (d, J=1.83
Hz, 1H), 7.37 (d, J=1.83 Hz, 1H), 7.35 (t, J=2.56 Hz, 1H), 6.85
(broad s, 2H), 6.56 (dd, J.sub.1=1.83 Hz, J.sub.2=3.10 Hz, 1H).
[0104] Compound VI: A solution of
N''-cyano-N-(7-iodo-1H-indol-5-yl)guanidine V (6.08 g, 18.7 mmol)
in 2-methoxyethyl ether (50 mL) was heated to 175.degree. C. for
32.5 h. The reaction mixture was cooled to 25.degree. C., the
resulting solids removed by filtration and washed with methanol.
The filtrate was concentrated in vacuo to give a brown oil. The
residue was dissolved in methanol and then absorbed onto Merck
Silica gel 60, 230-400 mesh (25 g). Flash chromatography (Merck
Silica gel 60, 230-400 mesh, 90/10/1 methylene
chloride/methanol/ammonium hydroxide) afforded
6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine VI (3.61 g, 59%) as
a brown solid: .sup.1H NMR (DMSO-d.sub.6, 300 MHz) .delta. 11.36
(broad s, 1H), 7.45 (broad s, 1H), 7.43 (t, J=2.93 Hz, 1H), 7.20
(s, 1H), 6.74 (broad s, 2H), 5.78 (broad s, 2H). ##STR20##
[0105] Compound VII: The coupling reaction can be carried out by a
conventional aryl coupling method, e.g., Suzuki coupling method:
(a) Suzuki et al., synth.commun. 1981, 11, 513, (b) Suzuki pure and
Appl. Chem. 1985, 57, 1749-1758, (c) Suzuki et al., Chem. Rev.
1995, 95, 2457-2483, (d) Shieh et al., J. Org. Chem. 1992, 57,
379-381, (e) Martin et al., Acta Chemica Scandinavica. 1993, 47,
513.
[0106] Typical conditions used to carry out the Suzuki coupling of
6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine VI includes the use
of either aryl or heteroaromatic boronic acid or esters (e.g.,
where Ar is defined as aryl) as coupling partner, in aqueous base
such as sodium bicarbonate or potassium carbonate or barium
hydroxide or triethylamine solution, a palladium catalyst (2-20
mole %) such as tetrakis(triphenylphosphine)-palladium (o) or
[1,1'bis(diphenylphosphino)-ferrocene]dichloro-palladium(II), in a
suitable solvent such as aqueous ethanol or THF or DMF or ethylene
glycol for at temperatures ranging from 25.degree. C. to
125.degree. C. for 2-18 hr yields compound VII.
[0107] Alternatively, coupling reaction can be carried out by a
conventional aryl or heteroaromatic coupling partner utilizing
Stille coupling, e.g., Stille et al., Angew. Chem. Int. Ed. Engl.,
1986, 25, 508.
[0108] Typical conditions used to carry out the Stille reaction
include the use of an organostannane as the coupling partner,
palladium catalyst (2-20 mole %) such as
tetrakis(triphenylphosphine)-palladium (o) or
[1,1'bis(diphenylphosphino)-ferrocene]dichloro-palladium(II), a
salt such as potassium fluoride or lithium chloride, in a suitable
anhydrous solvent such as THF or DMF or ethylene glycol for at
temperatures ranging from 25.degree. C. to 125.degree. C. for 2-18
hr yields compound VII. ##STR21##
[0109] Compound VIII: A solution of
6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine VI, 400 mg, 1.23
mmol) in tetrahydrofuran (20 mL) at 25.degree. C. was treated with
sodium hydroxide (98 mg, 2.46 mmol), methyl iodide (0.09 mL, 1.48
mmol), and tetrabutylammonium bromide (198 mg, 0.62 mmol), and the
resulting mixture stirred at 25.degree. C. for 18 h. The reaction
mixture was treated with ethyl acetate, water, and a saturated
aqueous sodium chloride solution, shaken and separated. The aqueous
layer was extracted with ethyl acetate, and the combined organic
layers were dried over sodium sulfate, filtered, and concentrated
in vacuo to afford
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine (500 mg)
as a yellow solid. The product was taken on into the next reaction
without further purification
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine VIII.
[0110] Compound IX: The coupling reaction can be carried out by a
conventional aryl coupling method, e.g., Suzuki coupling method:
(a) Suzuki et al., synth.commun. 1981, 11, 513, (b) Suzuki pure and
Appl. Chem. 1985, 57, 1749-1758, (c) Suzuki et al., Chem. Rev.
1995, 95, 2457-2483, (d) Shieh et al., J. Org. Chem. 1992, 57,
379-381, (e) Martin et al., Acta Chemica Scandinavica. 1993, 47,
513.
[0111] Typical conditions used to carry out the Suzuki coupling of
VIII includes the use of either aryl or heteroaromatic boronic acid
or esters (e.g., where Ar is defined as aryl) as coupling partner,
in aqueous base such as sodium bicarbonate or potassium carbonate
or barium hydroxide or triethylamine solution, a palladium catalyst
(2-20 mole %) such as tetrakis(triphenylphosphine)-palladium (o) or
[1,1'-bis(diphenylphosphino)-ferrocene]dichloro-palladium(II), in a
suitable solvent such as aqueous ethanol or THF or DMF or ethylene
glycol for at temperatures ranging from 25.degree. C. to
125.degree. C. for 2-18 hr yields
6-Aryl-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine X.
[0112] Alternatively, coupling reaction can be carried out by a
conventional aryl or heteroaromatic coupling partner utilizing
Stille coupling, e.g., Stille et al., Angew. Chem. Int. Ed. Engl.,
1986, 25, 508.
[0113] Typical conditions used to carry out the Stille reaction
include the use of an organostannane as the coupling partner,
palladium catalyst (2-20 mole %) such as
tetrakis(triphenylphosphine)-palladium (o) or
[1,1'bis(diphenylphosphino)-ferrocene]dichloro-palladium(II), a
salt such as potassium fluoride or lithium chloride, in a suitable
anhydrous solvent such as THF or DMF or ethylene glycol for at
temperatures ranging from 25.degree. C. to 125.degree. C. for 2-18
hr yields compound
6-Aryl-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine IX.
##STR22##
[0114] Compound X: Typical condition used to carry out alkylation
of 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine VI and phase
transfer catalyst such as tetrabutylammonium bromide, with variety
of halides (e.g. RaBr or RaI, where Ra is defined above) is carried
out with suitable solvent such as tetrahydrofuran, DMF using
suitable base such as sodium hydroxide at temperatures ranging from
-78.degree. C. to 25.degree. C. to provide the
6-iodo-7-alkyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine XI.
[0115] 6-Aryl-7-alkyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine XI:
The coupling reaction can be carried out by a conventional aryl
coupling method, e.g., Suzuki coupling method: (a) Suzuki et al.,
synth.commun. 1981, 11, 513, (b) Suzuki, Pure and Appl. Chem. 1985,
57, 1749-1758, (c) Suzuki et al., Chem. Rev. 1995, 95, 2457-2483,
(d) Shieh et al., J. Org. Chem. 1992, 57, 379-381, (e) Martin et
al., Acta Chemica Scandinavica. 1993, 47, 513.
[0116] Typical conditions used to carry out the Suzuki coupling of
6-iodo-7-alkyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine X includes
the use of either aryl or heteroaromatic boronic acid or esters
(e.g. where Ar is defined as aryl) as coupling partner, in aqueous
base such as sodium bicarbonate or potassium carbonate or barium
hydroxide or triethylamine solution, a palladium catalyst (2-20
mole %) such as tetrakis(triphenylphosphine)-palladium (o) or
[1,1'bis(diphenylphosphino)-ferrocene]dichloro-palladium(II), in a
suitable solvent such as aqueous ethanol or THF or DMF or ethylene
glycol for at temperatures ranging from 25.degree. C. to
125.degree. C. for 2-18 hr yields compound X.
[0117] Alternatively, coupling reaction can be carried out by a
conventional aryl or heteroaromatic coupling partner utilizing
Stille coupling. e.g., Stille et al., Angew. Chem. Int. Ed. Engl.,
1986, 25, 508.
[0118] Typical conditions used to carry out the Stille reaction
include the use of an organostannane as the coupling partner,
palladium catalyst (2-20 mole %) such as
tetrakis(triphenylphosphine)-palladium (o) or
[1,1'bis(diphenylphosphino)-ferrocene]dichloro-palladium(II), a
salt such as potassium fluoride or lithium chloride, in a suitable
anhydrous solvent such as THF or DMF or ethylene glycol for at
temperatures ranging from 25.degree. C. to 125.degree. C. for 2-18
hr yields 6-Aryl-7-alkyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
XI.
[0119] This invention is illustrated by the following Examples. In
the Examples, the procedures of Examples 2-28 were carried out by
the procedure of Example 1. In the Examples, the procedures of
Examples 30-33 were carried out by the procedure of Example 29. In
the Examples, the procedures of Examples 35-104 were carried out by
the procedure of Example 34. In the Examples, the procedures of
Examples 106-112 were carried out by the procedure of Example 105.
In the Examples, the procedure of Example 114 was carried out by
the procedure of Example 113.
EXAMPLES
Example 1
6-(3,5-Bis-trifluoromethyl-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamin-
e
[0120] ##STR23##
[0121] A solution of
6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine (322 mg, 0.99 mmol)
in ethylene glycol dimethyl ether (3.0 mL) and ethanol (3.0 mL)at
25.degree. C. was treated with 3,5-bis(trifluoromethyl)benzene
boronic acid (510 mg, 1.98 mmol), a saturated aqueous sodium
bicarbonate solution (1.5 mL), and
tetrakis(triphenylphosphine)-palladium (o) (115 mg, 0.1 mmol). The
resulting mixture was heated to 80.degree. C. for 18 h, cooled,
filtered and the isolated solids washed with ethyl acetate. The
filtrate was pre-absorbed onto silica gel and purified by flash
chromatography (Merck Silica gel 60, 230-400 mesh, 90/10/1
methylene chloride/methanol/ammonium hydroxide) to give
6-(3,5-bis-trifluoromethyl-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diami-
ne (218 mg, 53.5%) as a yellow solid; EI-HRMS m/e calcd for
C.sub.18H.sub.11F.sub.6N.sub.5 (M.sup.+) 411.0918, found
411.0921.
[0122] In an analogous manner, there were obtained:
Example 2
[0123] ##STR24##
[0124] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
3-ethoxyphenylboronic acid there was produced
6-(3-Ethoxy-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.18H.sub.17N.sub.5O
(M+H).sup.+ at m/z=320.
Example 3
[0125] ##STR25##
[0126] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2-ethoxyphenylboronic acid there was produced
6-(2-Ethoxy-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.18H.sub.17N.sub.5O
(M+H).sup.+ at m/z=320.
Example 4
[0127] ##STR26##
[0128] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
3-nitrophenylboronic acid there was produced
6-(3-Nitro-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine;
EI-HRMS m/e calcd for C.sub.16H.sub.12N.sub.6O.sub.2 (M.sup.+)
320.1022, found 320.1020.
Example 5
[0129] ##STR27##
[0130] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2,5-dichlorophenylboronic acid there was produced
6-(2,5-Dichloro-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine;
EI-HRMS m/e calcd for C.sub.16H.sub.11Cl.sub.2N.sub.5 (M.sup.+)
343.0391, found 343.0392.
Example 6
[0131] ##STR28##
[0132] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
5-chlorothiophene-2-boronic acid there was produced
6-(5-Chloro-thiophen-2-yl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; (ES).sup.+-HRMS m/e calcd for
C.sub.14H.sub.10ClN.sub.5S (M+H) 316.0418, found 316.0422.
Example 7
[0133] ##STR29##
[0134] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
o-tolylboronic acid there was produced
6-o-Tolyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine as an off-white
solid; EI-HRMS m/e calcd for C.sub.17H.sub.15N.sub.5 (M+H).sup.+
290.1400, found 290.1399.
Example 8
[0135] ##STR30##
[0136] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
3-aminobenzeneboronic acid there was produced
6-(3-Amino-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.16H.sub.14N.sub.6 (M+H).sup.+ at m/z=291.
Example 9
[0137] ##STR31##
[0138] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
4-fluorophenylboronic acid there was produced
6-(4-Fluoro-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.16H.sub.12FN.sub.5 (M+H).sup.+ at m/z=294.
Example 10
[0139] ##STR32##
[0140] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
3-methylphenylboronic acid there was produced
6-m-Tolyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine trifluoro-acetic
acid salt as a white solid;. LRMS for C.sub.17H.sub.15N.sub.5
(M+H).sup.+ at m/z=290
Example 11
[0141] ##STR33##
[0142] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
4-biphenylphenylboronic acid there was produced
6-Biphenyl-4-yl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.22H.sub.17N.sub.5 (M+H).sup.+ at m/z=352.
Example 12
[0143] ##STR34##
[0144] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
4-methyl-3-nitrophenylboronic acid there was produced
6-(4-methyl-3-nitro-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.17H.sub.14N.sub.6O.sub.2 (M+H).sup.+ at m/z=335.
Example 13
[0145] ##STR35##
[0146] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
3-fluorophenylboronic acid there was produced
6-(3-Fluoro-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.16H.sub.12FN.sub.5 (M+H).sup.+ at m/z=294.
Example 14
[0147] ##STR36##
[0148] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
4-ethylphenylboronic acid there was produced
6-(4-Ethyl-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.18H.sub.17N.sub.5 (M+H).sup.+ at m/z=335.
Example 15
[0149] ##STR37##
[0150] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
4-tert-butylbenzeneboronic acid there was produced
6-(4-tert-Butyl-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.20H.sub.21N.sub.5 (M+H).sup.+ at m/z=332.
Example 16
[0151] ##STR38##
[0152] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
(3-isopropylphenyl)boronic acid there was produced
6-(3-Isopropyl-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt a white solid; LRMS for
C.sub.19H.sub.19N.sub.5 (M+H).sup.+ at m/z=318.
Example 17
[0153] ##STR39##
[0154] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
benzo(B)thiophene-2-boronic acid there was produced
6-Benzo[b]thiophen-2-yl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as white solid; LRMS for
C.sub.18H.sub.13N.sub.5S (M+H).sup.+ at m/z=332.
Example 18
[0155] ##STR40##
[0156] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2,4-dichlorophenylboronic acid there was produced
6-(2,4-Dichloro-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.16H.sub.11Cl.sub.2N.sub.5 (M+H).sup.+ at m/z=344.
Example 19
[0157] ##STR41##
[0158] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
1-naphthaleneboronic acid there was produced
6-Naphthalen-1-yl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.20H.sub.15N.sub.5 (M+H).sup.+ at m/z=326.
Example 20
[0159] ##STR42##
[0160] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
3,5-dichlorophenylboronic acid there was produced
6-(3,5-Dichloro-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.16H.sub.11Cl.sub.2N.sub.5 (M+H).sup.+ at m/z=344.
Example 21
[0161] ##STR43##
[0162] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
naphthalene-2-boronic acid there was produced
6-Naphthalen-2-yl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.20H.sub.15N.sub.5 (M+H).sup.+ at m/z=326.
Example 22
[0163] ##STR44##
[0164] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2-chlorophenylboronic acid there was produced
6-(2-Chloro-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.16H.sub.12ClN.sub.5 (M+H).sup.+ at m/z=310.
Example 23
[0165] ##STR45##
[0166] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2,4-dimethoxyphenylboronic acid there was produced
6-(2,4-Dimethoxy-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.18H.sub.17N.sub.5O.sub.2 (M+H).sup.+ at m/z=336.
Example 24
[0167] ##STR46##
[0168] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
5-acetyl-2-thiopheneboronic acid there was produced
1-[5-(1,3-Diamino-7H-pyrrolo[3,2-f]quinazolin-6-yl)-thiophen-2-yl]-ethano-
ne trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.16H.sub.13N.sub.5OS (M+H).sup.+ at m/z=324.
Example 25
[0169] ##STR47##
[0170] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
3-formylphenylboronic acid there was produced
3-(1,3-Diamino-7H-pyrrolo[3,2-f]quinazolin-6-yl)-benzaldehyde as a
yellow solid; (ES).sup.+-HRMS m/e calcd for
C.sub.17H.sub.13N.sub.5O (M+H).sup.+ 304.1193, found 304.1195.
Example 26
[0171] ##STR48##
[0172] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
5-chloro-2-methoxyphenylboronic acid there was produced
6-(5-Chloro-2-methoxy-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.17H.sub.14ClN.sub.5O
(M+H).sup.+ at m/z=340.
Example 27
[0173] ##STR49##
[0174] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
(3-acetylaminophenyl)boronic acid there was produced
N-[3-(1,3-Diamino-7H-pyrrolo[3,2-f]quinazolin-6-yl)-phenyl]-acetamide
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.18H.sub.16N.sub.6O (M+H).sup.+ at m/z=333.
Example 28
[0175] ##STR50##
[0176] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2-(trifluoromethylbenzene)boronic acid there was produced
6-(2-Trifluoromethyl-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
as a light brown solid; LRMS for C.sub.17H.sub.12F.sub.3N.sub.5
(M+H).sup.+ at m/z=344.
Example 29
3-[2-(1,3-Diamino-7H-pyrrolo[3,2-f]quinazolin-6-yl)-phenyl]-propionic
acid
[0177] ##STR51##
[0178] A mixture of 3-(2-bromo-phenyl)-propionic acid (458 mg, 2.0
mmol),
4,4,5,5,4',4',5',5'-octamethyl-[2,2']bi[[1,3,2]dioxaborolanyl] (558
mg, 2.20 mmol),
[1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium (II) (132
mg, 0.18 mmol), and potassium acetate (589 mg, 6.0 mmol) was heated
to 95.degree. C. for 2 d. The resulting mixture was diluted with
water and extracted with ethyl acetate. The combined organic layers
were washed with a saturated aqueous sodium chloride solution,
filtered through a pad of silca gel and sodium sulfate, and
concentrated in vacuo to afford
3-[2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-propionic
acid. A solution of 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
(prepared as in Example 1, 100 mg, 0.31 mmol),
3-[2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-propionic
acid (102 mg, 0.37 mmol), tetrakis(triphenylphosphine)palladium(o)
(71 mg, 0.06 mmol) in a 2.0M aqueous sodium carbonate solution (0.5
mL), ethanol (1.5 mL), and ethylene glycol dimethyl ether (1.5 mL)
was heated to 95.degree. C. for 18 h. The resulting mixture was
cooled to 25.degree. C., dissolved in methanol and tetrahydrofuran,
and filtered through a pad of silica gel and sodium sulfate. The
filtrate was concentrated in vacuo. HPLC purification (Shimadzu
HPLC, ODSA column from Medchem, 2.times.10 cm, 10 micro, 10-90%
CH3CN/H.sub.2O with 0.1% TFA.) afforded
3-[2-(1,3-diamino-7H-pyrrolo[3,2-f]quinazolin-6-yl)-phenyl]-propionic
acid (12.5 mg, 12.1%); LRMS for C.sub.19H.sub.17N.sub.5O.sub.2
(M+H).sup.+ at m/z=348.
[0179] In an analogous manner, there were obtained:
Example 30
[0180] ##STR52##
[0181] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
[3-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-acetic
acid there was produced
[3-(1,3-Diamino-7H-pyrrolo[3,2-f]quinazolin-6-yl)-phenyl]-acetic
acid; LRMS for C.sub.18H.sub.15N.sub.5O.sub.2 (M+H).sup.+ at
m/z=334.
Example 31
[0182] ##STR53##
[0183] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
[4-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-acetic
acid there was produced
[4-(1,3-Diamino-7H-pyrrolo[3,2-f]quinazolin-6-yl)-phenyl]-acetic
acid; LRMS for C.sub.18H.sub.15N.sub.5O.sub.2 (M+H).sup.+ at
m/z=334.
Example 32
[0184] ##STR54##
[0185] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
3-[3-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-propionic
acid there was produced
3-[3-(1,3-Diamino-7H-pyrrolo[3,2-f]quinazolin-6-yl)-phenyl]-propionic
acid; LRMS for C.sub.19H.sub.17N.sub.5O.sub.2 (M+H).sup.+ for
m/z=348.
Example 33
[0186] ##STR55##
[0187] From 6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
3-[4-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-propionic
acid there was produced
3-[4-(1,3-Diamino-7H-pyrrolo[3,2-f]quinazolin-6-yl)-phenyl]-propionic
acid; LRMS for C.sub.19H.sub.17N.sub.5O.sub.2 (M+H).sup.+ at
m/z=348.
Example 34
[0188] ##STR56##
6-(2,6-Dimethyl-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
[0189] A solution of
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine (1.68 g,
5.00 mmol) in ethylene glycol dimethyl ether (10 mL) at 25.degree.
C. was treated with 2,6-dimethylbenzene boronic acid (1.50 g, 10.0
mmol) in ethanol (10 mL), sodium bicarbonate (2.84 g, 26.80 mmol),
and tetrakis(triphenylphosphine)-palladium (o) (3.31 g, 2.86 mmol).
The resulting mixture was heated to 80.degree. C. for 3 h. The
resulting mixture was filtered through a pad of celite and the
filtrate diluted with water (100 mL). This solution was extracted
with a 95/5/0.5 solution of methylene chloride/methanol/ammonium
hydroxide (3.times.100 mL) and the combined organic layers dried
over magnesium sulfate, filtered, and concentrated in vacuo. Flash
chromatography (Merck Silica gel 60, 230-400 mesh, 90/5/0.5
methylene chloride/methanol/ammonium hydroxide) afforded
6-(2,6-dimethyl-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
(100 mg, 6.34%) as an off-white solid; EI-HRMS m/e calcd for
C.sub.19H.sub.19N.sub.5 (M.sup.+) 317.1640, found 317.1632.
[0190] In an analogous manner, there were obtained:
Example 35
[0191] ##STR57##
[0192] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
3,4-methylenedioxyphenylboronic acid there was produced
6-Benzo[1,3]dioxol-5-yl-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.18H.sub.15N.sub.5O.sub.2
(M+H).sup.+ at m/z=334.
Example 36
[0193] ##STR58##
[0194] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
3-aminobenzeneboronic acid there was produced
6-(3-Amino-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.17H.sub.16N.sub.6 (M+H).sup.+ at m/z=305.
Example 37
[0195] ##STR59##
[0196] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
4-fluorophenylboronic acid there was produced
6-(4-Fluoro-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.17H.sub.14FN.sub.5 (M+H).sup.+ at m/z=308.
Example 38
[0197] ##STR60##
[0198] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
3-methylphenylboronic acid there was produced
7-Methyl-6-m-tolyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.18H.sub.17N.sub.5 (M+H).sup.+ at m/z=304.
Example 39
[0199] ##STR61##
[0200] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
4-biphenylboronic acid there was produced
6-Biphenyl-4-yl-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.23H.sub.19N.sub.5 (M+H).sup.+ at m/z=366.
Example 40
[0201] ##STR62##
[0202] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
4-methyl-3-nitrophenylboronic acid there was produced
7-methyl-6-(4-methyl-3-nitro-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-dia-
mine trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.18H.sub.16N.sub.6O.sub.2 (M+H).sup.+ for m/z=349.
Example 41
[0203] ##STR63##
[0204] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
3-fluorophenylboronic acid there was produced
6-(3-Fluoro-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.17H.sub.14FN.sub.5 (M+H).sup.+ at m/z=308.
Example 42
[0205] ##STR64##
[0206] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
4-ethylphenylboronic acid there was produced
6-(4-Ethyl-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.19H.sub.19N.sub.5 (M+H).sup.+ at m/z=318.
Example 43
[0207] ##STR65##
[0208] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
(3-isopropylphenyl)boronic acid there was produced
6-(3-Isopropyl-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.20H.sub.21N.sub.5 (M+H).sup.+ at m/z=332.
Example 44
[0209] ##STR66##
[0210] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
benzo[B]thiphene-2-boronic acid there was produced
6-Benzo[b]thiophen-2-yl-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.19H.sub.15N.sub.5S (M+H).sup.+ at m/z=346.
Example 45
[0211] ##STR67##
[0212] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2,4-dichlorophenylboronic acid there was produced
6-(2,4-Dichloro-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.17H.sub.13Cl.sub.2N.sub.5 (M+H).sup.+ at m/z=358.
Example 46
[0213] ##STR68##
[0214] From 6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3diamine
and 1-naphthaleneboronic acid there was produced
7-Methyl-6-naphthalen-1-yl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.21H.sub.17N.sub.5 (M+H).sup.+ at m/z=340.
Example 47
[0215] ##STR69##
[0216] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
3,5-dichlorophenylboronic acid there was produced
6-(3,5-Dichloro-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.17H.sub.13Cl.sub.2N.sub.5 (M+H).sup.+ at m/z=358.
Example 48
[0217] ##STR70##
[0218] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
(3-acetylaminophenyl)boronic acid there was produced
N-[3-(1,3-Diamino-7-methyl-7H-pyrrolo[3,2-f]quinazolin-6-yl)-phenyl]-acet-
amide trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.19H.sub.18N.sub.6O (M+H).sup.+ at m/z=347.
Example 49
[0219] ##STR71##
[0220] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
naphthalene-2-boronic acid there was produced
7-Methyl-6-naphthalen-2-yl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.21H.sub.17N.sub.5 (M+H).sup.+ at m/z=340.
Example 50
[0221] ##STR72##
[0222] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2-chlorophenylboronic acid there was produced
6-(2-Chloro-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.17H.sub.14ClN.sub.5 (M+H).sup.+ at m/z=324.
Example 51
[0223] ##STR73##
[0224] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2,4-dimethoxyphenylboronic acid there was produced
6-(2,4-Dimethoxy-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamin-
e trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.19H.sub.19N.sub.5O.sub.2 (M+H).sup.+ at m/z=350.
Example 52
[0225] ##STR74##
[0226] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
3-acetylphenylboronic acid there was produced
1-[3-(1,3-Diamino-7-methyl-7H-pyrrolo[3,2-f]quinazolin-6-yl)-phenyl]-etha-
none trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.19H.sub.17N.sub.5O (M+H).sup.+ at m/z=332.
Example 53
[0227] ##STR75##
[0228] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
5-acetyl-2-thiopheneboronic acid there was produced
1-[5-(1,3-Diamino-7-methyl-7H-pyrrolo[3,2-f]quinazolin-6-yl)-thiophen-2-y-
l]-ethanone trifluoro-acetic acid salt as a white solid; LRMS for
C.sub.17H.sub.15N.sub.5OS (M+H).sup.+ at m/z=338.
Example 54
[0229] ##STR76##
[0230] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
(3-hydroxymethylphenyl)boronic acid there was produced
[3-(1,3-Diamino-7-methyl-7H-pyrrolo[3,2-f]quinazolin-6-yl)-phenyl]-methan-
ol trifluoro-acetic acid salt; LRMS for C.sub.18H.sub.17N.sub.5O
(M+H).sup.+ at m/z=320.
Example 55
[0231] ##STR77##
[0232] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2,3-dimethylphenylboronic acid there was produced
6-(2,3-Dimethyl-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.19H.sub.19N.sub.5
(M+H).sup.+ at m/z=318.
Example 56
[0233] ##STR78##
[0234] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2,5-difluorophenylboronic acid there was produced
6-(2,5-Difluoro-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.17H.sub.13F.sub.2N.sub.5
(M+H).sup.+ at m/z=326.
Example 57
[0235] ##STR79##
[0236] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
5-fluoro-2-methoxyphenylboronic acid there was produced
6-(5-Fluoro-2-methoxy-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-d-
iamine trifluoro-acetic acid salt; LRMS for
C.sub.18H.sub.16FN.sub.5O (M+H).sup.+ at m/z=338.
Example 58
[0237] ##STR80##
[0238] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2,5-dimethoxyphenylboronic acid there was produced
6-(2,5-Dimethoxy-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamin-
e trifluoro-acetic acid salt; LRMS m/z calcd for
C.sub.19H.sub.19N.sub.5O.sub.2 (M+H).sup.+ at m/z=350.
Example 59
[0239] ##STR81##
[0240] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2-acetylphenylboronic acid there was produced
1-[2-(1,3-Diamino-7-methyl-7H-pyrrolo[3,2-f]quinazolin-6-yl)-phenyl]-etha-
none trifluoro-acetic acid salt; LRMS for C.sub.19H.sub.17N.sub.5O
(M+H).sup.+ at m/z=332.
Example 60
[0241] ##STR82##
[0242] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
5-chlorothiophene-2-boronic acid there was produced
6-(5-Chloro-thiophen-2-yl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diam-
ine trifluoro-acetic acid salt; LRMS for C.sub.15H.sub.12ClN.sub.5S
(M+H).sup.+ at m/z=330.
Example 61
[0243] ##STR83##
[0244] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
furan-2-boronic acid there was produced
6-Furan-2-yl-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.15H.sub.13N.sub.5O
(M+H).sup.+ at m/z=280.
Example 62
[0245] ##STR84##
[0246] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
5-methylthiophene-2-boronic acid there was produced
7-Methyl-6-(5-methyl-thiophen-2-yl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diam-
ine as an off-white solid; EI-HRMS m/e calcd. for
C.sub.16H.sub.15N.sub.5S (M+H).sup.+ 310.1121, found 310.1125.
Example 63
[0247] ##STR85##
[0248] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
4-acetylphenylboronic acid there was produced
1-[4-(1,3-Diamino-7-methyl-7H-pyrrolo[3,2-f]quinazolin-6-yl)-phenyl]-etha-
none trifluoro-acetic acid salt; LRMS for C.sub.19H.sub.17N.sub.5O
(M+H).sup.+ at m/z=332.
Example 64
[0249] ##STR86##
[0250] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
3,4-dimethoxyphenylboronic acid there was produced
6-(3,4-Dimethoxy-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamin-
e trifluoro-acetic acid salt; LRMS for
C.sub.19H.sub.19N.sub.5O.sub.2 (M+H).sup.+ at m/z=350.
Example 65
[0251] ##STR87##
[0252] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
4-(trifluoromethoxy)benzeneboronic acid there was produced
7-Methyl-6-(4-trifluoromethoxy-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-d-
iamine trifluoro-acetic acid salt; LRMS for
C.sub.18H.sub.14F.sub.3N.sub.5O (M+H).sup.+ at m/z=374.
Example 66
[0253] ##STR88##
[0254] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2,6-difluorophenylboronic acid there was produced
6-(2,6-Difluoro-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.17H.sub.13F.sub.2N.sub.5
(M+H).sup.+ at m/z=326.
Example 67
[0255] ##STR89##
[0256] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
3,4-dichlorophenylboronic acid there was produced
6-(3,4-Dichloro-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for
C.sub.17H.sub.13Cl.sub.2N.sub.5 (M+H).sup.+ at m/z=358.
Example 68
[0257] ##STR90##
[0258] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
4-bromophenylboronic acid there was produced
6-(4-Bromo-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.17H.sub.14BrN.sub.5
(M+H).sup.+ at m/z=368.
Example 69
[0259] ##STR91##
[0260] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
3-nitrophenylboronic acid there was produced
7-methyl-6-(3-nitro-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.17H.sub.14N.sub.6O.sub.2
(M+H).sup.+ at m/z=335.
Example 70
[0261] ##STR92##
[0262] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
4-(ethylthio)phenylboronic acid there was produced
6-(4-Ethylsulfanyl-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diam-
ine trifluoro-acetic acid salt; LRMS for C.sub.19H.sub.19N.sub.5S
(M+H).sup.+ at m/z=350.
Example 71
[0263] ##STR93##
[0264] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
4-(methylthio)phenylboronic acid there was produced
7-Methyl-6-(4-methylsulfanyl-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-dia-
mine trifluoro-acetic acid salt; LRMS for C.sub.18H.sub.17N.sub.5S
(M+H).sup.+ at m/z=336.
Example 72
[0265] ##STR94##
[0266] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
4-methylphenylboronic acid there was produced
7-Methyl-6-p-tolyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.18H.sub.17N.sub.5
(M+H).sup.+ at m/z=304.
Example 73
[0267] ##STR95##
[0268] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
4-chlorophenylboronic acid there was produced
6-(4-Chloro-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.17H.sub.14ClN.sub.5
(M+H).sup.+ at m/z=324.
Example 74
[0269] ##STR96##
[0270] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
3,5-dimethylisoxazole-4-boronic acid there was produced
6-(3,5-Dimethyl-isoxazol-4-yl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3--
diamine trifluoro-acetic acid salt; LRMS for
C.sub.16H.sub.16N.sub.6O (M+H).sup.+ at m/z=309.
Example 75
[0271] ##STR97##
[0272] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
benzothiophene-7-boronic acid there was produced
6-(3,5-6-Benzo[b]thiophen-7-yl-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3--
diamine trifluoro-acetic acid salt; LRMS for
C.sub.19H.sub.15N.sub.5S (M+H).sup.+ at m/z=346.
Example 76
[0273] ##STR98##
[0274] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
phenoxathin-4-boronic acid there was produced
7-Methyl-6-phenoxathiin-4-yl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.23H.sub.17N.sub.5OS
(M+H).sup.+ at m/z=412.
Example 77
[0275] ##STR99##
[0276] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2-fluorophenylboronic acid there was produced
6-(2-Fluoro-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.17H.sub.14FN.sub.5
(M+H).sup.+ at m/z=308.
Example 78
[0277] ##STR100##
[0278] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2,4-difluorobenzeneboronic acid there was produced
6-(2,4-Difluoro-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.17H.sub.13F.sub.2N.sub.5
(M+H).sup.+ at m/z=326.
Example 79
[0279] ##STR101##
[0280] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2,5-dimethylphenylboronic acid there was produced
6-(2,5-Dimethyl-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.19H.sub.19N.sub.5
(M+H).sup.+at m/z=318.
Example 80
[0281] ##STR102##
[0282] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2,3-dichlorophenylboronic acid there was produced
6-(2,3-Dichloro-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for
C.sub.17H.sub.13Cl.sub.2N.sub.5 (M+H).sup.+ at m/z=358.
Example 81
[0283] ##STR103##
[0284] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2-formyl-3-thiopheneboronic acid there was produced
3-(1,3-Diamino-7-methyl-7H-pyrrolo[3,2-f]quinazolin-6-yl)-thiophene-2-car-
baldehyde trifluoro-acetic acid salt; LRMS for
C.sub.16H.sub.13N.sub.5OS (M+H).sup.+ at m/z=324.
Example 82
[0285] ##STR104##
[0286] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
(4-hydroxyphenyl)boronic acid there was produced
4-(1,3-Diamino-7-methyl-7H-pyrrolo[3,2-f]quinazolin-6-yl)-phenol
trifluoro-acetic acid salt; LRMS for C.sub.17H.sub.15N.sub.5O
(M+H).sup.+ at m/z=306.
Example 83
[0287] ##STR105##
[0288] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
1-benzothiophen-3-ylboronic acid there was produced
6-Benzo[b]thiophen-3-yl-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.19H.sub.15N.sub.5S
(M).sup.+ at m/z=345.
Example 84
[0289] ##STR106##
[0290] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
(2-nitrophenyl)boronic acid there was produced
7-methyl-6-(2-nitro-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.17H.sub.14N.sub.6O.sub.2
(M+H).sup.+ at m/z=335.
Example 85
[0291] ##STR107##
[0292] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
5-isopropyl-2-methoxybenzeneboronic acid there was produced
6-(5-Isopropyl-2-methoxy-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,-
3-diamine trifluoro-acetic acid salt; LRMS for
C.sub.21H.sub.23N.sub.5O (M+H).sup.+ at m/z=362.
Example 86
[0293] ##STR108##
[0294] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
(3-hydroxyphenyl)boronic acid there was produced
3-(1,3-Diamino-7-methyl-7H-pyrrolo[3,2-f]quinazolin-6-yl)-phenol
trifluoro-acetic acid salt; LRMS for C.sub.17H.sub.15N.sub.5O
(M+H).sup.+ at m/z=306.
Example 87
[0295] ##STR109##
[0296] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2-(phenoxy)phenylboronic acid there was produced
7-Methyl-6-(2-phenoxy-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.23H.sub.19N.sub.5O
(M+H).sup.+ at m/z=382.
Example 88
[0297] ##STR110##
[0298] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
3-chlorophenylboronic acid there was produced
6-(3-Chloro-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.17H.sub.14ClN.sub.5
(M+H).sup.+ at m/z=324.
Example 89
[0299] ##STR111##
[0300] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
o-tolylboronic acid there was produced
7-Methyl-6-o-tolyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.18H.sub.17N.sub.5
(M+H).sup.+ at m/z=304.
Example 90
[0301] ##STR112##
[0302] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
4-vinylphenylboronic acid there was produced
7-Methyl-6-(4-vinyl-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.19H.sub.17N.sub.5
(M+H).sup.+ at m/z=316.
Example 91
[0303] ##STR113##
[0304] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
4-ethoxyphenylboronic acid there was produced
6-(4-Ethoxy-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.19H.sub.19N.sub.5O
(M+H).sup.+ at m/z=334.
Example 92
[0305] ##STR114##
[0306] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
3-chloro-4-fluorophenylboronic acid there was produced
6-(3-Chloro-4-fluoro-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-di-
amine trifluoro-acetic acid salt; LRMS for
C.sub.17H.sub.13ClFN.sub.5 (M+H).sup.+ at m/z=342.
Example 93
[0307] ##STR115##
[0308] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
4-methoxyphenylboronic acid there was produced
6-(4-Methoxy-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt; LRMS for C.sub.18H.sub.17N.sub.5O
(M+H).sup.+ at m/z=320.
Example 94
[0309] ##STR116##
[0310] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
4-bromo-2-fluorobenzeneboronic acid there was produced
6-(4-Bromo-2-fluoro-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-dia-
mine trifluoro-acetic acid salt; LRMS for
C.sub.17H.sub.13BrFN.sub.5 (M+H).sup.+ at m/z=386.
Example 95
[0311] ##STR117##
[0312] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2,6-dimethoxyphenylboronic acid there was produced
6-(2,6-Dimethoxy-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamin-
e trifluoro-acetic acid salt; LRMS for
C.sub.19H.sub.19N.sub.5O.sub.2 (M+H).sup.+ at m/z=350.
Example 96
[0313] ##STR118##
[0314] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2-tert-butoxycarbonyl-4-methoxyphenylboronic acid there was
produced
2-(1,3-Diamino-7-methyl-7H-pyrrolo[3,2-f]quinazolin-6-yl)-5-methoxy-benzo-
ic acid trifluoro-acetic acid salt; LRMS for
C.sub.19H.sub.17N.sub.5O.sub.3 (M+H).sup.+ at m/z=364.
Example 97
[0315] ##STR119##
[0316] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
5-methoxy thiopheneboronic acid there was produced
6-(5-Methoxy-thiophen-2-yl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-dia-
mine as a light yellow solid; EI-HRMS m/e calcd for
C.sub.16H.sub.15N.sub.5OS (M.sup.+) 325.0997, found 325.0994.
Example 98
[0317] ##STR120##
[0318] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2-methoxyphenylboronic acid there was produced
6-(2-Methoxy-phenyl)-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
as a light brown solid; LRMS for C.sub.18H.sub.17N.sub.5O
(M+H).sup.+ at m/z=320.
Example 99
[0319] ##STR121##
[0320] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
thiophene-2-boronic acid there was produced
7-Methyl-6-thiophen-2-yl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
as a light yellow solid; LRMS for C.sub.15H.sub.13N.sub.5S
(M+Na).sup.+ at m/z=318.
Example 100
[0321] ##STR122##
[0322] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
benzo[B]furan-2-boronic acid there was produced
6-Benzofuran-2-yl-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
as a yellow solid; LRMS for C.sub.19H.sub.15N.sub.5O (M+H).sup.+ at
m/z=330.
Example 101
[0323] ##STR123##
[0324] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
2-(trifluoromethyl)benzeneboronic acid there was produced
7-Methyl-6-(2-trifluoromethyl-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-di-
amine as a yellow solid; LRMS for C.sub.18H.sub.14F.sub.3N.sub.5
(M+H).sup.+ at m/z=358.
Example 102
[0325] ##STR124##
[0326] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
[3-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-acetic
acid there was produced
[3-(1,3-Diamino-7-methyl-7H-pyrrolo[3,2-f]quinazolin-6-yl)-phenyl]-acetic
acid; LRMS for C.sub.19H.sub.17N.sub.5O.sub.2 (M+H).sup.+ at
m/z=348.
Example 103
[0327] ##STR125##
[0328] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
3-[2-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-propionic
acid there was produced
3-[2-(1,3-Diamino-7-methyl-7H-pyrrolo[3,2-f]quinazolin-6-yl)-phenyl]-prop-
ionic acid; LRMS for C.sub.20H.sub.19N.sub.5O.sub.2 (M+H).sup.+ at
m/z=362.
Example 104
[0329] ##STR126##
[0330] From
6-iodo-7-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine and
3-[3-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-propionic
acid there was produced
3-[3-(1,3-Diamino-7-methyl-7H-pyrrolo[3,2-f]quinazolin-6-yl)-phenyl]-prop-
ionic acid; LRMS for C.sub.20H.sub.19N.sub.5O.sub.2 (M+H).sup.+ at
m/z=362.
Example 105
7-Methanesulfonyl-6-thiophen-2-yl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoro-acetic acid salt
[0331] ##STR127##
[0332] To a slurry of
6-Thiophen-2-yl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine (example
100), prepared as described in example 1 from
6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine VI and
2-thiopheneboronic acid, (50 mg, 0.178 mmole) in anhydrous DMF (3
ml) at room temperature was added sodium hydride (60% in mineral
oil, 8 mg, 0.20 mmole) and the mixture was stirred at room
temperature for 45 minutes. The above mixture was cooled in an ice
bath, methanesulfonyl chloride was slowly added dropwise (0.016 ml,
0.207 mmole) and stirred at 0.degree. C. for 30 minutes. The
mixture was then warmed up to room temperature and stirred
overnight. Additional amounts of sodium hydride (8 mg) and
methanesulfonyl chloride (0.016 ml) was added the next day to drive
the reaction to completion and the mixture was stirred at room
temperature for an additional 20 hours. The mixture was evaporated
to dryness and the crude mixture was purified by reversed phase
HPLC to give
7-Methanesulfonyl-6-thiophen-2-yl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamin-
e trifluoro-acetic acid salt as a light brown solid; LRMS m/z calcd
for C.sub.15H.sub.13N.sub.5O.sub.2S.sub.2 (M+H).sup.+ at
m/z=360.
Example 106
[0333] ##STR128##
[0334] From
2-(1,3-Diamino-6-iodo-pyrrolo[3,2-f]quinazolin-7-yl)-ethanol and
2-(trifluoromethyl)benzeneboronic acid there was produced
2-[1,3-Diamino-6-(2-trifluoromethyl-phenyl)-pyrrolo[3,2-f]quinazolin-7-yl-
]-ethanol trifluoro-acetic acid salt as an off-white solid; LRMS
for C.sub.19H.sub.16F.sub.3N.sub.5O (M+H).sup.+ at m/z=388.
Example 107
[0335] ##STR129##
[0336] From
(1,3-Diamino-6-iodo-pyrrolo[3,2-f]quinazolin-7-yl)-acetic acid and
2-(trifluoromethyl)benzeneboronic acid there was produced
[1,3-Diamino-6-(2-trifluoromethyl-phenyl)-pyrrolo[3,2-f]quinazolin-7-yl]--
acetic acid trifluoro-acetic acid salt as an off-white solid; LRMS
for C.sub.19H.sub.14F.sub.3N.sub.5O.sub.2 (M+H).sup.+ at
m/z=402.
Example 108
[0337] ##STR130##
[0338] From
(1,3-Diamino-6-iodo-pyrrolo[3,2-f]quinazolin-7-yl)-acetic acid and
thiophene-2-boronic acid there was produced
(1,3-Diamino-6-thiophen-2-yl-pyrrolo[3,2-f]quinazolin-7-yl)-acetic
acid trifluoro-acetic acid salt as an off-white solid; LRMS for
C.sub.16H.sub.13N.sub.5O.sub.2S (M+H).sup.+ at m/z=340.
Example 109
[0339] ##STR131##
[0340] From
7-(2-Benzyloxy-ethyl)-6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
and 2-(trifluoromethyl)benzeneboronic acid there was produced
7-(2-Benzyloxy-ethyl)-6-(2-trifluoromethyl-phenyl)-7H-pyrrolo[3,2-f]quina-
zoline-1,3-diamine trifluoro-acetic acid salt as a light brown
solid; LRMS for C.sub.26H.sub.22F.sub.3N.sub.5O (M+H).sup.+ at
m/z=478.
Example 110
[0341] ##STR132##
[0342] From
2-(1,3-Diamino-6-iodo-pyrrolo[3,2-f]quinazolin-7-yl)-N,N-diethyl-acetamid-
e and 3-methoxyphenylboronic acid there was produced
2-[1,3-Diamino-6-(3-methoxy-phenyl)-pyrrolo[3,2-f]quinazolin-7-yl]-N,N-di-
ethyl-acetamide as a yellow solid; LRMS for
C.sub.23H.sub.26N.sub.6O.sub.2 (M+H).sup.+ at m/z=419.
Example 111
[0343] ##STR133##
[0344] From 7-Ethyl-6-iodo-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
and thiophene-2-boronic acid there was produced
7-Ethyl-6-thiophen-2-yl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine as
an off-white solid; .sup.1H NMR (DMSO-d.sub.6, 300 MHz) .delta.
7.69 (d, J=5.13 Hz, 1H), 7.49 (d, J=2.56 Hz, 1H), 7.27 (m, 1H),
7.18 (m, 1H), 7.14 (d, J=2.56 Hz, 1H), 6.91 (s, 1H), 6.81 (broad s,
2H), 5.82 (broad s, 2H), 3.82 (q, J=6.96 Hz, 2H), 0.99 (t, J=6.96
Hz, 3H).
Example 112
[0345] ##STR134##
[0346] From
6-Iodo-7-(2-methoxy-ethyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
and 3-methoxyphenylboronic acid there was produced
7-(2-Methoxy-ethyl)-6-(3-methoxy-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-
-diamine as a light-brown solid; LRMS for
C.sub.20H.sub.21N.sub.5O.sub.2 (M+H).sup.+ at m/z=364.
[0347] Scheme 5 is directed to the synthesis of 8 methyl
derivatives. ##STR135##
Example 113
8-Methyl-6-thiophen-2-yl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
trifluoroacetic acid salt
[0348] ##STR136##
[0349] To a cooled (0-10C) mixture of concentrated nitric acid (12
mL) and concentrated sulfuric acid (40 mL) was added
1-acetyl-2-methyl-indoline XII (12.5 g, 0.0713 moles), prepared by
an analgous method to that described in Chem.Ber.; 14; 1881; 890,
in small portions so that the internal temperature of the reaction
remained between 10-20.degree. C. The resulting mixture was allowed
to stir at 5-10.degree. C. overnight. The mixture was poured slowly
into 300 mL of cold water and the precipitate that formed was
collected by filtration, washed with water and redissolved in an
ethanol-6N HCl solution and warmed to reflux for 30 minutes. The
resulting solution was concentrated, EtOAc was added and the Ph of
the solution adjusted to 10. The organic phase was separated and
dried over MgSO.sub.4. The mixture was filtered, and evaporated and
the crude material purified by column chromatography (50%
EtOAc-Hexane) to give 3.31 g, 26% of
2-methyl-5-nitro-2,3-dihydro-1H-indole XIII: LRMS for
C.sub.9H.sub.10N.sub.2O.sub.2 (M+H).sup.+ at m/z=179.
[0350] A mixture of silver sulfate (4.92 g, 0.0157 mol) and iodine
(4 g, 0.0.0157 mol) in N,N-dimethylformamide (50 mL) and ethanol
(100 mL) was treated with 2-methyl-5-nitro-2,3-dihydro-1H-indole
XIII (3.31 g, 0.015 mol) and the resulting mixture was stirred at
25.degree. C. for 30 min before an additional 1 g of iodine was
added and the stirring continued for 2 h. The resulting reaction
mixture was filtered and the solids washed with ethyl acetate
before being concentrated in vacuo to a volume of approximately 50
mL. This solution was treated with a 1.0N aqueous sodium
thiosulfate solution (100 mL) and a saturated aqueous sodium
chloride solution (200 mL). The resulting precipitate was collected
by filtration, washed with water and petroleum ether, and dried in
vacuo to 7-iodo-2-methyl-5-nitro-2,3-dihydro-1H-indole XIV as a
yellow solid: LRMS for C.sub.9H.sub.9IN.sub.2O.sub.2 (M+H).sup.+ at
m/z=305.
[0351] A solution of 7-iodo-2-methyl-5-nitro-2,3-dihydro-1H-indole
XIV (4.75 g, 0.0156 mol) in methanol (150 mL) at 25.degree. C. was
treated with a solution of ammonium chloride (5.22 g, 0.0976 mol)
in water (150 mL) and iron powder (3 g, 0.0534 mol). The mixture
was heated to 100.degree. C. under a nitrogen atmosphere for 6 h.
The reaction mixture was filtered hot through a pad of celite and
washed with hot methanol. The filtrate was concentrated in vacuo
and the residue partitioned between methylene chloride and water.
The layers were separated and the pH of the aqueous layer was
adjusted to pH=10 with ammonium hydroxide. The aqueous layer was
extracted with methylene chloride and the combined organic layers
were dried over sodium sulfate, filtered, and concentrated in vacuo
to a volume of 50 mL. The resulting solution was treated with a
4.0M aqueous hydrochloric acid solution in dioxane and then stirred
at 25.degree. C. for 1 h. The precipitate was collected by
filtration and washed with methylene chloride and petroleum ether
to afford 7-iodo-2-methyl-1H-indol-5-ylamine hydrochloride XV (4.37
g, 81%) as a gray solid: LRMS for freebase C.sub.9H.sub.11IN.sub.2
(M+H).sup.+ at m/z=275.
[0352] A solution of 7-iodo-2-methyl-1H-indol-5-ylamine
hydrochloride XV (4.3 g, 12.39 mmol) in methanol (200 mL) at
25.degree. C. was treated with
2,3-dichloro-5,6-dicyano-1,4-benzoquinone (2.8 g, 12.39 mmol) in
portions. The resulting dark solution was concentrated in vacuo and
partitioned between water and methylene chloride, the pH was
adjusted to 10 by the addition of with ammonium hydroxide, the
organic layer separated and filtered and the aqueous layer
extracted 3.times.100 mL with methylene chloride. The organic
layers were combined, dried over magnesium sulfate and charcoal.
The mixture was filtered and concentrated to 100 mL in volume
before 20 mL of a 4.0 M HCL in dioxane solution was added. The
resulting mixture was stirred at room temperature for 1 h and the
precipitate formed was isolated by filtration, washed well with
ether and dried to give 7-iodo-2-methyl-1H-indol-5-ylamine
hydrochloride XVI (1.94 g, 58%) as a grey solid: LRMS for freebase
C.sub.9H.sub.9IN.sub.2 (M+H).sup.+ at m/z=273.
[0353] A solution of 7-iodo-2-methyl-1H-indol-5-ylamine
hydrochloride XVII (1.9 g, 6.158 mmol) in NN-dimethylformamide (30
mL) at 25.degree. C. was treated with sodium dicyanamide (1.37 g,
15.397 mmol) and then warmed to 45.degree. C. for 4 h. The
resulting mixture filtered and concentrated in vacuo and the
residue treated with water (20 mL). The resulting mixture was
allowed to stand at 25.degree. C. for 2.5 h during which time a
solid formed. The solid was collected by filtration and washed with
water, resuspended in methanol, filtered and dried to give
N''-cyano-N-(7-iodo-2-methyl-1H-indol-5-yl)guanidine XVIII (0.88 g,
42%) as a light grey solid: LRMS for C.sub.11H.sub.10IN.sub.5
(M-H).sup.+ at m/z=338.
[0354] A solution of
N''-cyano-N-(7-iodo-2-methyl-1H-indol-5-yl)guanidine XVIII (0.86 g,
2.54 mmol) in 2-methoxyethyl ether (20 mL) was heated to
175.degree. C. for 28 h. The reaction mixture was cooled to
25.degree. C. and the solid formed was removed by filtration and
washed with methanol. The filtrate was concentrated in vacuo and
the residue triturated with methanol and ether to give a brown
solid which was isolated by filtration and dried to give
6-iodo-8-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine XIX (120
mg, 14%) as a brown solid: LRMS for C.sub.11H.sub.10IN.sub.5
(M+H).sup.+ at m/z=340.
[0355] A solution of
6-iodo-8-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine XIX (20
mg, 0.06 mmol) in ethylene glycol dimethyl ether (5.0 mL) and
ethanol (2.5 mL) at 25.degree. C. was treated with
2-thiopheneboronic acid (11 mg, 0.09 mmol), a 2 M aqueous sodium
carbonate solution (2.5 mL), and
tetrakis(triphenylphosphine)-palladium (o) (0.3 mg, 0.0026 mmol).
The resulting mixture was heated to 80.degree. C. for 3 h, cooled
and pre-absorbed onto silica gel and purified by flash
chromatography (Merck Silica gel 60, 230-400 mesh, 90/10/1
methylene chloride/methanol/ammonium hydroxide) followed by
reversed phase HPLC (Zorbax 21.2.times.100 mmSB C18 column, 15 min
95/5 to 5/95 water/acetonitrile 0.075% TFA gradient) to afford
8-Methyl-6-thiophen-2-yl-7H-pyrrolo[3,2-f]quinazoline-1,3-diami- ne
trifluoro-acetic acid salt XX (4 mg, 25%) as a lyophilized solid;
LRMS for freebase C.sub.15H.sub.13N.sub.5S.sub.2 (M+H).sup.+ at
m/z=296.
[0356] In an analogous manner, there were obtained:
Example 114
[0357] ##STR137##
[0358] From
6-iodo-8-methyl-7H-pyrrolo[3,2-f]quinazoline-1,3-diamine
2-(trifluoromethylbenzene)boronic acid
8-Methyl-6-(2-trifluoromethyl-phenyl)-7H-pyrrolo[3,2-f]quinazoline-1,3-di-
amine as a lyophilized solid; LRMS for
C.sub.18H.sub.14F.sub.3N.sub.5 (M+H).sup.+ at m/z=358.
Example 115
In vitro inhibition of PTP1B
Enzymes
[0359] Human PTP1B (1-321) was cloned from a human cDNA library
using conventional molecular biology techniques. The cDNA sequence
was identical to the published human PTP1B sequence (Accession
number M33689). The protein was expressed and purified from E. coli
as described by Barford D. et.al, J. Mol Biol (1994) 239,
726-730).
Example 116
PTPase Assays
[0360] The measurement of PTPase activity was carried out using one
of two methods:
[0361] The first method for the measurement of PTP1B inhibitory
activity a tyrosine phosphorylated peptide based on the amino acid
sequence of insulin receptor tyrosine autophosphorylation site 1146
(TRDI(pY)E) was used as substrate. The reaction conditions were as
follows:
[0362] PTP1B (0.5-2 nM) was incubated with compound for 15 min
buffer containing 37.5 mM Bis-Tris buffer pH 6.2, 140 mMNaCl, 0.05%
BSA and 2 mM DTT. The reaction was started by the addition of 50
.mu.M substrate. After 20 min at room temperature (22-25.degree.
C.) the reaction was stopped with KOH and the amount of free
phosphate measured using Malachite Green as previously described.
(Harder et al. 1994 Biochem J. 298; 395).
[0363] The second method was used for the measurement of general
PTPase inhibitory activity across a panel of PTPases the substrate
(6,8-difluoro-4-methylumbelliferyl phosphate (DiFMUP; from
Molecular Probes) was used at the Km for each enzyme. The buffer
conditions were identical as in the Malachite Green assay. The
reaction was stopped with KOH. In this case the dephosphoryated
product becomes fluorescent and the fluorescence read.
(Excitiation:360 mM/Emmission: 460 nM).
[0364] For kinetic experiments the same buffer conditions were used
except that the reaction was started using enzyme and the reaction
stopped after 10 minutes.
[0365] The IC.sub.50 values (in .mu.M) for the PTP1B inhibitory
activity of the compounds in the present application are in the
range of 5.20 .mu.M to 96.3 .mu.M. The most preferred compounds
shown an IC.sub.50 of <30.0 .mu.M.
[0366] Examples of the some compounds with its corresponding
IC.sub.50 values are TABLE-US-00001 Example IC.sub.50 (.mu.M) 2
23.79 4 89.52 6 29.22 8 24.11
Example 117
Glucose Uptake Assay
[0367] The day before the assay the SKMC media was changed to high
glucose DMEM, 25 mM Hepes, pH 7.0 and 2% Charcoal/dextran treated
FBS for 19 hours.
[0368] On the morning of the assay, cells were starved for max. 2
hours in low glucose (5.5 mM glucose) DMEM, 25 mM Hepes, pH 7.0 and
0.5% BSA. The starvation meduim was removed and replaced with test
medium (150 mMNaCl, 25 mM Hepes, pH 7.0) containing either 1% DMSO,
or test compound diluted in DMSO or Porcine Insulin to a final
concentrations of 1, 0.1, 0.05, 0.01 and 0.01 .mu.M. Each assay
point was performed in triplicate. The cells were incubated for 45
min at 37.degree. C. 10 .mu.M Cytochalasin B (CB) was added to
appropriate wells to stop the active glucose transport (i.e GLUT 1
& 4). At this point 2-Deoxy-D(U-.sup.14C) glucose (Amersham,
Code CFB.sub.195, 200 uCi/ml) was added to all wells to a final
concentration of 0.8 .mu.Ci/ml. The cells were incubated for an
additional 45 minutes at 37.degree. C. in an incubator. Cells were
then very gently washed for three times in PBS (RT). The cells were
then lysed with the addition of 0.05% NaOH solution for 20 min at
RT. The lysate was transferred to a scintillation vial containing 5
ml of scintillatio fluid and counted in a Beckman LS6500
Scintillation counter. Analysis of results: The counts obtained
with CB (passive glucose transport values) were subtracted from
every value obtained with PI (or compounds) in order to evalute
only active glucose transport. Fold increase was calculated by
dividing values in the presence of PI (or compounds) by the value
obtained in the presence of DMSO (control). Compounds were
considered to be active when they increase glucose uptake at least
25% of the Porcine Insulin response at 0.05 .mu.M.
Example 118
[0369] In vivo inhibition of PTP1B: Effects of compounds on blood
glucose levels in mouse model
[0370] To measure the anti-diabetic effect compounds were tested in
well established rodent in vivo models of type 2 diabetes and
obesity.
Diet Induced Obese C.57BL6/J Mice (DIO Mice)
[0371] Mice that have type 2 diabetes were be generated by
maintaining them on a high fat diet for a 4-6 months (Diabetes vol.
37 September 1988). Male C57B16/J mice (age 3-4 weeks) were placed
on high fat diet for 4-6 months. At this time, they were
hyperglycemic and hyperinsulinemic and weighed 40-50 g. DIO mice
(n=10) were weighed and fasted for a two hour period prior to oral
treatment. Immediately prior to dosing a pre-dose blood glucose
reading was taken by snipping off a portion of the tail and
collecting blood from the tail vein. Mice were treated either with
a single dose of compound (acute) or once a day for 5 days
(sub-chronic). For the acute studies glucose was generally measured
at 2 h, 4 h, 6 h, 8 h post treatment. Compounds were considered
active if they showed a statistically significant (p.ltoreq.0.05)
glucose lowering (>15%) compared to the vehicle treated
animals.
[0372] For sub-chronic (5 day) studies mice were dosed once a day
by gavage as described above. On day five, glucose was measured
prior to dosing (0 time) and 2 hours after dosing. Insulin and
triglycerides were measured at 2 hour post dose. Compounds were
considered active if they showed a statistically significant
(p.ltoreq.0.05) glucose, insulin and triglyceride lowering compared
to the vehicle treated animals.
* * * * *