U.S. patent application number 14/626320 was filed with the patent office on 2015-06-11 for tetrahydropyrrolothiazine compounds.
The applicant listed for this patent is Eli Lilly and Company. Invention is credited to Steven James GREEN, Dustin James MERGOTT, Brian Morgan WATSON, Leonard Larry WINNEROSKI, JR..
Application Number | 20150157641 14/626320 |
Document ID | / |
Family ID | 50382615 |
Filed Date | 2015-06-11 |
United States Patent
Application |
20150157641 |
Kind Code |
A1 |
GREEN; Steven James ; et
al. |
June 11, 2015 |
TETRAHYDROPYRROLOTHIAZINE COMPOUNDS
Abstract
The present invention provides a compound of Formula I:
##STR00001## wherein R is H or F; and A is: ##STR00002## or a
pharmaceutically acceptable salt thereof.
Inventors: |
GREEN; Steven James;
(Indianapolis, IN) ; MERGOTT; Dustin James;
(Zionsville, IN) ; WATSON; Brian Morgan;
(Indianapolis, IN) ; WINNEROSKI, JR.; Leonard Larry;
(Greenwood, IN) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Eli Lilly and Company |
Indianapolis |
IN |
US |
|
|
Family ID: |
50382615 |
Appl. No.: |
14/626320 |
Filed: |
February 19, 2015 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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14453855 |
Aug 7, 2014 |
8987254 |
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14626320 |
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14195897 |
Mar 4, 2014 |
8841293 |
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14453855 |
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61776819 |
Mar 12, 2013 |
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Current U.S.
Class: |
514/224.2 |
Current CPC
Class: |
A61P 43/00 20180101;
C07D 513/04 20130101; A61K 31/542 20130101; A61P 25/28 20180101;
A61P 25/00 20180101 |
International
Class: |
A61K 31/542 20060101
A61K031/542 |
Claims
1-5. (canceled)
6. A process for preparing a pharmaceutical composition, comprising
admixing a compound of the formula: ##STR00056## wherein R is H or
F; and A is: ##STR00057## or a pharmaceutically acceptable salt
thereof, with one or more pharmaceutically acceptable carriers,
diluents, or excipients.
7. The process according to claim 6 wherein the compound is:
##STR00058## or a pharmaceutically acceptable salt thereof.
8. The process according to claim 6 wherein the compound is the HCl
salt of: ##STR00059##
Description
[0001] The present invention relates to novel
tetrahydropyrrolothiazine compounds, to pharmaceutical compositions
comprising the compounds, to methods of using the compounds to
treat physiological disorders, and to intermediates and processes
useful in the synthesis of the compounds.
[0002] The present invention is in the field of treatment of
Alzheimer's disease and other diseases and disorders involving
amyloid .beta. (Abeta) peptide, a neurotoxic and highly aggregatory
peptide segment of the amyloid precursor protein (APP). Alzheimer's
disease is a devastating neurodegenerative disorder that affects
millions of patients worldwide. In view of the currently approved
agents on the market which afford only transient, symptomatic
benefits to the patient, there is a significant unmet need in the
treatment of Alzheimer's disease.
[0003] Alzheimer's disease is characterized by the generation,
aggregation, and deposition of Abeta in the brain. Complete or
partial inhibition of .beta.-secretase (.beta.-site amyloid
precursor protein-cleaving enzyme; BACE) has been shown to have a
significant effect on plaque-related and plaque-dependent
pathologies in mouse models suggesting that even small reductions
in A.beta. peptide levels might result in a long-term significant
reduction in plaque burden and synaptic deficits, thus providing
significant therapeutic benefits, particularly in the treatment of
Alzheimer's disease.
[0004] US 2009/0209755 discloses fused aminodihydrothiazine
derivatives which possess BACE inhibitory activity and are further
disclosed as useful therapeutic agents for a neurodegenerative
disease caused by A.beta. peptide, such as Alzheimer's type
dementia. In addition, J. Neuroscience, 31(46), pages 16507-16516
(2011) discloses
(S)-4-(2,4-difluoro-5-pyrimidin-5-yl-phenyl)-4-methyl-5,6-dihydro-4H-[1,3-
]thiazin-2-ylamine, an orally administered CNS-active BACE
inhibitor.
[0005] BACE inhibitors that are potent with sufficient CNS
penetration are desired to provide treatments for Abeta
peptide-mediated disorders, such as Alzheimer's disease. The
present invention provides certain novel compounds that are potent
inhibitors of BACE. In addition, the present invention provides
certain novel compounds with CNS penetration.
[0006] Accordingly, the present invention provides a compound of
Formula I:
##STR00003## [0007] wherein R is H or F; and [0008] A is:
##STR00004##
[0008] or a pharmaceutically acceptable salt thereof.
[0009] The present invention also provides a method of treating
Alzheimer's disease in a patient, comprising administering to a
patient in need of such treatment an effective amount of a compound
of Formula I, or a pharmaceutically acceptable salt thereof.
[0010] The present invention further provides a method of
preventing the progression of mild cognitive impairment to
Alzheimer's disease in a patient, comprising administering to a
patient in need of such treatment an effective amount of a compound
of Formula I, or a pharmaceutically acceptable salt thereof.
[0011] The present invention also provides a method of inhibiting
BACE in a patient, comprising administering to a patient in need of
such treatment an effective amount of a compound of Formula I, or a
pharmaceutically acceptable salt thereof.
[0012] The present invention also provides a method for inhibiting
BACE-mediated cleavage of amyloid precursor protein, comprising
administering to a patient in need of such treatment an effective
amount of a compound of Formula I, or a pharmaceutically acceptable
salt thereof.
[0013] The invention further provides a method for the inhibition
of production of Abeta peptide, comprising administering to a
patient in need of such treatment an effective amount of a compound
of Formula I, or a pharmaceutically acceptable salt thereof.
[0014] Furthermore, this invention provides a compound of Formula I
or a pharmaceutically acceptable salt thereof for use in therapy,
in particular for the treatment of Alzheimer's disease or for the
prevention of the progression of mild cognitive impairment to
Alzheimer's disease. Even furthermore, this invention provides the
use of a compound of Formula I, or a pharmaceutically acceptable
salt thereof, for the manufacture of a medicament for the treatment
of Alzheimer's disease. This invention also provides the use of a
compound of Formula I, or a pharmaceutically acceptable salt
thereof, for the manufacture of a medicament for the prevention of
the progression of mild cognitive impairment to Alzheimer's
disease. The invention also provides the use of a compound of
Formula I, or a pharmaceutically acceptable salt thereof, for the
manufacture of a medicament for the inhibition of B ACE. The
invention further provides the use of a compound of Formula I, or a
pharmaceutically acceptable salt thereof, for the manufacture of a
medicament for the inhibition of production of Abeta peptide.
[0015] The invention further provides a pharmaceutical composition,
comprising a compound of Formula I, or a pharmaceutically
acceptable salt thereof, in combination with one or more
pharmaceutically acceptable carriers, diluents, or excipients. In a
particular embodiment, the composition further comprises one or
more other therapeutic agents. This invention also encompasses
novel intermediates and processes for the synthesis of the
compounds of Formula I.
[0016] Mild cognitive impairment has been defined as a potential
prodromal phase of dementia associated with Alzheimer's disease
based on clinical presentation and on progression of patients
exhibiting mild cognitive impairment to Alzheimer's dementia over
time. (Morris, et al., Arch. Neurol., 58, 397-405 (2001); Petersen,
et al., Arch. Neurol., 56, 303-308 (1999)). The term "prevention of
the progression of mild cognitive impairment to Alzheimer's
disease" includes slowing, arresting, or reversing the progression
of mild cognitive impairment to Alzheimer's disease in a
patient.
[0017] As used herein, the terms "treating" or "to treat" includes
restraining, slowing, stopping, or reversing the progression or
severity of an existing symptom or disorder.
[0018] As used herein, the term "patient" refers to a human.
[0019] The term "inhibition of production of Abeta peptide" is
taken to mean decreasing of in vivo levels of Abeta peptide in a
patient.
[0020] As used herein, the term "effective amount" refers to the
amount or dose of compound of the invention, or a pharmaceutically
acceptable salt thereof which, upon single or multiple dose
administration to the patient, provides the desired effect in the
patient under diagnosis or treatment.
[0021] An effective amount can be readily determined by the
attending diagnostician, as one skilled in the art, by the use of
known techniques and by observing results obtained under analogous
circumstances. In determining the effective amount for a patient, a
number of factors are considered by the attending diagnostician,
including, but not limited to: the species of patient; its size,
age, and general health; the specific disease or disorder involved;
the degree of or involvement or the severity of the disease or
disorder; the response of the individual patient; the particular
compound administered; the mode of administration; the
bioavailability characteristics of the preparation administered;
the dose regimen selected; the use of concomitant medication; and
other relevant circumstances.
[0022] The compounds of the present invention are generally
effective over a wide dosage range. For example, dosages per day
normally fall within the range of about 0.01 to about 20 mg/kg of
body weight. In some instances dosage levels below the lower limit
of the aforesaid range may be more than adequate, while in other
cases still larger doses may be employed with acceptable side
effects, and therefore the above dosage range is not intended to
limit the scope of the invention in any way.
[0023] The compounds of the present invention are preferably
formulated as pharmaceutical compositions administered by any route
which makes the compound bioavailable, including oral and
parenteral routes. Most preferably, such compositions are for oral
administration. Such pharmaceutical compositions and processes for
preparing same are well known in the art. (See, e.g., Remington:
The Science and Practice of Pharmacy (D. B. Troy, Editor, 21st
Edition, Lippincott, Williams & Wilkins, 2006).
[0024] One of ordinary skill in the art will appreciate that
compounds of the invention can exist in tautomeric forms, as
depicted in Scheme A. When any reference in this application to one
of the specific tautomers of the compounds of the invention is
given, it is understood to encompass both tautomeric forms and all
mixtures thereof.
##STR00005##
[0025] The compounds of the present invention, or salts thereof,
may be prepared by a variety of procedures known in the art, some
of which are illustrated in the Schemes, Preparations, and Examples
below. The specific synthetic steps for each of the routes
described may be combined in different ways, or in conjunction with
steps from different schemes, to prepare compounds of Formula I, or
salts thereof. The products of each step in the schemes below can
be recovered by conventional methods, including extraction,
evaporation, precipitation, chromatography, filtration,
trituration, and crystallization.
[0026] Certain stereochemical centers have been left unspecified
and certain substituents have been eliminated in the following
schemes for the sake of clarity and are not intended to limit the
teaching of the schemes in any way. Furthermore, individual
isomers, enantiomers, or diastereomers may be separated or resolved
by one of ordinary skill in the art at any convenient point in the
synthesis of compounds of Formula I by methods such as selective
crystallization techniques or chiral chromatography (See for
example, J. Jacques, et al., "Enantiomers, Racemates, and
Resolutions", John Wiley and Sons, Inc., 1981, and E. L. Eliel and
S. H. Wilen, "Stereochemistry of Organic Compounds",
Wiley-Interscience, 1994). The designations "isomer 1" and "isomer
2" refer to the compounds that elute from chiral chromatography
first and second, respectively, and if chiral chromatography is
initiated early in the synthesis, the same designation is applied
to subsequent intermediates and examples. Additionally, the
intermediates described in the following schemes contain a number
of nitrogen protecting groups. The variable protecting group may be
the same or different in each occurrence depending on the
particular reaction conditions and the particular transformations
to be performed. The protection and deprotection conditions are
well known to the skilled artisan and are described in the
literature (See for example "Greene's Protective Groups in Organic
Synthesis", Fourth Edition, by Peter G. M. Wuts and Theodora W.
Greene, John Wiley and Sons, Inc. 2007).
[0027] One of ordinary skill in the art will appreciate that
compounds of the invention are comprised of a core that contains at
least two chiral centers:
##STR00006##
Although the present invention contemplates all individual
enantiomers, as well as mixtures of the enantiomers of said
compounds, including racemates, the compounds with the absolute
configuration at the carbon atoms labeled 1 and 2 as illustrated in
Scheme B are preferred compounds of the invention.
[0028] Abbreviations used herein are defined according to
Aldrichimica Acta, Vol. 17, No. 1, 1984. Other abbreviations are
defined as follows: "APP" refers to amyloid precursor protein;
"BOC" refers to tert-butyloxycarbonyl; "CSF" refers to
cerebrospinal fluid; "DCC" refers to 1,3-dicyclohexylcarbodiimide;
"DIC" refers to diisopropylcarbodiimide; "DMEM" refers to
Dulbecco's Modified Eagle's Medium; "DMSO" refers to dimethyl
sulfoxide; "EDCI" refers to
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; "ee"
refers to enantiomeric excess; "EtOAc" refers to ethyl acetate;
"Ex" refers to example; "F12" refers to Ham's F12 medium; "FBS"
refers to Fetal Bovine Serum; "FRET" refers to fluorescence
resonance energy transfer; "HEK" refers to human embryonic kidney;
"HOAc" refers to acetic acid; "HOAt" refers to
1-hydroxy-7-azobenzotriazole; "HOBt" refers to
1-hydroxylbenzotriazole hydrate; "HPLC" refers to high-performance
liquid chromatography; "hr refers to hour or hours; "IC.sub.50"
refers to the concentration of an agent that produces 50% of the
maximal inhibitory response possible for that agent; "min" refers
to minute or minutes; "MTBE" refers to methyl tert-butyl ether;
"PDAPP" refers to platelet derived amyloid precursor protein;
"Prep" refers to preparation; "RFU" refers to relative fluorescence
unit "R.sub.t" refers to retention time; "RT" refers to room
temperature; "SCX" refers to strong cation exchange; "SFC" refers
to supercritical fluid chromatography; and "THF" refers to
tetrahydrofuran.
[0029] In the schemes below, all substituents unless otherwise
indicated, are as previously defined. The reagents and starting
materials are generally readily available to one of ordinary skill
in the art. Others may be made by standard techniques of organic
and heterocyclic chemistry which are analogous to the syntheses of
known structurally-similar compounds and the procedures described
in the Preparations and Examples which follow including any novel
procedures.
##STR00007##
[0030] Scheme 1 depicts the formation of oximes (4) and (8). The
oximes can each be used to form the bicyclic isoxazole (5). The
substituted aromatic group can be inserted at different points of
the synthesis as shown in Scheme 1, Step 1 and Step 7. "PG" is a
protecting group developed for the amino group, such as carbamates
and allyl. Such groups are well known and appreciated in the
art.
[0031] In a 2-step reaction, a ketone with a beta halogen (1) can
be alkylated (3, Step 1) with a protected allyl amine (2) using an
inorganic base such as potassium carbonate and then treated with
hydroxylamine hydrochloride and an organic base such as pyridine in
a polar protic solvent such as ethanol to give the oxime (4, Step
2). The oxime (4) can then be converted to the bicyclic isoxazole
(5) in a 3+2 cyclization by several methods such as heating the
oxime (4) in a non-polar solvent such as toluene or xylenes to form
the bicyclic isoxazole (5, Step 3). Alternatively, an oxime can be
formed starting from a dimethyl acetal (6) which is treated with an
acid such as formic acid to form the aldehyde (7, Step 4). In step
5, the aldehyde (7) can then be converted to the oxime (8) with
hydroxylamine hydrochloride and a base such as sodium acetate
trihydrate. The bicyclic isoxazole (9) can be formed from the oxime
(8) as shown in Step 6 using an aqueous solution of sodium
hypochlorite. In step 7, the protected bicyclic isoxazole (9) is
then reacted with an aromatic organolithium reagent or Grignard
reagent to give protected bicyclic isoxazole (5).
##STR00008##
[0032] Scheme 2 illustrates different routes to the protected
pyrrolo thiazine (12). The protected bicyclic isoxazole (5) can be
treated with powdered Zn in acetic acid or by Raney Nickel in a
polar solvent such as ethanol under pressure hydrogenation
conditions to give an aminopyrrolidine methanol (13, Step 11). The
aminopyrrolidine methanol (13) is then reacted with benzoyl
isothiocyanate in a polar solvent such as THF followed by the
addition of 1,1 carbonyldiimidazole (CDI) to give the fused
protected pyrrolidine thiazine (12, Step 12). Alternatively, the
amine of the bicyclic isoxazole (5) can be reacted with benzoyl
isothiocyanate to give the thiourea (10, Step 8), and then, in Step
9 the isoxazole ring can be opened with powdered zinc in acetic
acid to give the hydroxyl compound (11). The hydroxyl compound (11)
can then be treated with CDI in a polar aprotic solvent such as THF
or 1-chloro-N,N,2-trimethylpropenylamine in DCM to form the fused
protected pyrrolidine thiazine (12, Step 10). The fused pyrrolidine
thiazine (12) can also be formed from a Mitsunobu reaction such as
using triphenylphosphine and diisopropyl azodicarboxylate
(DIAD).
##STR00009##
[0033] Scheme 3 depicts the conversion of the pyrrolo thiazine (12)
to the aniline (14, Step 13) which can then be acylated followed by
the deprotection and heteroarylation of the pyrrolidine.
Deprotection of the thiazine amine leads to compounds of Formula
I.
[0034] Azido-dehalogenation is performed on the appropriate pyrrolo
thiazine (12) in the presence of an azide source, such as sodium
azide. Such azido-dehalogenation reactions are well known and
appreciated in the art. Reduction of the resulting azide
intermediate to the aniline (14, Step 13) may be effected by
hydrogenation conditions that are well known and described in the
art or by reducing agents well known in the art, such as
LiAlH.sub.4, NaBH.sub.4, PPh.sub.3.
[0035] A BOC protected pyrrolidine can be deprotected under acidic
conditions well known in the art (Step 1 of Step 14). The
deprotected pyrrolidine can then be heteroarylated in a
nucleophilic aromatic substitution (SNAr) with a substituted
aromatic pyrimidine using an organic base such as
diisopropylethylamine, triethylamine, or
N,N,N,N'-tetramethylguanidine to give compound 15 (Step 2 of Step
14). The aniline (15) can be coupled with heteroaromatic carboxylic
acids (16) under coupling conditions (Step 1 of Step 15). One
skilled in the art will recognize that there are a number of
methods and reagents for amide formation resulting from the
reaction of carboxylic acids and amines. For example, the reaction
of an appropriate aniline (15) with an appropriate acid of compound
16 in the presence of a coupling reagent and an amine base such as
DIPEA or triethylamine, will give a compound of Formula I following
deprotection of the thiazine amine. Coupling reagents include
carbodiimides such as DCC, DIC, EDCI, and aromatic oximes such as
HOBt and HOAt. Additionally, uronium or phosphonium salts of
non-nucleophilic anions such as HBTU, HATU, PyBOP, and PyBrOP can
be used in place of the more traditional coupling reagents.
Additives such as DMAP may be used to enhance the reaction.
Alternatively, the protected aniline amine (15) can be acylated
using substituted benzoyl chlorides in the presence of a base such
as triethylamine or pyridine. The protected thiazine amine can then
be deprotected with an organic base such as pyridine and
methylhydroxylamine hydrochloride in a polar aprotic solvent such
as ethanol or an inorganic base such as lithium hydroxide in
methanol to give compounds of Formula I.
[0036] In an optional step, a pharmaceutically acceptable salt of a
compound of Formula I can be formed by reaction of an appropriate
free base of Formula I with an appropriate pharmaceutically
acceptable acid in a suitable solvent under standard conditions.
Additionally, the formation of such salts can occur simultaneously
upon deprotection of a nitrogen protecting group. The formation of
such salts is well known and appreciated in the art. See, for
example, Gould, P. L., "Salt selection for basic drugs,"
International Journal of Pharmaceutics, 33: 201-217 (1986); Bastin,
R. J., et al. "Salt Selection and Optimization Procedures for
Pharmaceutical New Chemical Entities," Organic Process Research and
Development, 4: 427-435 (2000); and Berge, S. M., et al.,
"Pharmaceutical Salts," Journal of Pharmaceutical Sciences, 66:
1-19, (1977). One of ordinary skill in the art will appreciate that
a compound of Formula I is readily converted to and may be isolated
as a pharmaceutically acceptable salt, such as a hydrochloride
salt.
PREPARATIONS AND EXAMPLES
[0037] The following preparations and examples further illustrate
the invention. Unless noted to the contrary, the compounds
illustrated herein are named and numbered using Symyx.RTM. Draw
version 3.2 or version 4.0 (Symyx Solutions, Inc.) or IUPACNAME
ACDLABS.
Preparation 1
1-(3-Bromophenyl)-2-(diallylamino)ethanone
##STR00010##
[0039] Potassium carbonate (38.8 g, 281 mmol) is added to
3-bromophenacyl bromide (60 g 216 mmol) in acetonitrile (430 mL),
and the mixture is cooled under nitrogen to 0.degree. C.
Diallylamine (34.6 mL, 280.63 mmol) is added drop wise over 1 hour
and the reaction is allowed to warm to 22.degree. C. overnight. The
crude reaction mixture is concentrated and the residue is
partitioned in water (300 mL) and MTBE (300 mL). The aqueous layer
is discarded and the organic layer is washed with water (100 mL,
2.times.) and with brine (100 mL). The organic layer is dried over
sodium sulfate, filtered, and the solvent evaporated to constant
weight to give the title compound (62 g, 98%). ES/MS (m/e): 294
(M+1).
Preparation 2
Benzyl N-(2,2-dimethoxyethyl)carbamate
##STR00011##
[0041] A solution of aminoacetaldehyde dimethyl acetal (25 mL, 229
mmol) in toluene (120 mL) is treated at 0.degree. C. with a 4.85 M
sodium hydroxide solution (70.8 mL, 343.5 mmol). The mixture is
stirred at 0.degree. C. for 10 minutes and benzyl chloroformate
(33.8 mL, 229 mmol) is added keeping the internal temperature below
20.degree. C. during the addition. The mixture is warmed to room
temperature over 4 hours. The organic layer is separated, washed
with brine, dried over sodium sulfate, and concentrated to dryness
to give the title compound (54 g, 98%). ES/MS (m/e): 240 (M+H).
Preparation 3
Benzyl N-allyl-N-(2,2-dimethoxyethyl)carbamate
##STR00012##
[0043] A solution of benzyl N-(2,2-dimethoxyethyl)carbamate (50 g,
208.9 mmol) in toluene (180 mL) is treated with solid potassium
hydroxide (51.6 g, 919.69 mmol) under nitrogen. After 10 minutes,
benzyltriethylammonium chloride (0.8 g, 3.1 mmol) is added. After
another 10 minutes a solution of allyl bromide (33 g, 272.8 mmol)
in toluene (50 mL) is added drop wise over 10 minutes. The
resultant mixture is stirred at 50.degree. C. for 48 hours. The
mixture is cooled to room temperature and quenched with water. The
organic layer is separated, washed with brine, dried over magnesium
sulfate, and concentrated to dryness to give the title compound (44
g, 75%). ES/MS (m/e): 280 (M+H).
Preparation 4
Benzyl N-allyl-N-(2-oxoethyl)carbamate
##STR00013##
[0045] A solution of benzyl N-allyl-N-(2,2-dimethoxyethyl)carbamate
(30 g, 107 mmol) in formic acid (36.8 mL, 860 mmol) and water (4.84
mL) is stirred at room temperature overnight. The mixture is
concentrated and diluted with hexanes/ethyl acetate (1:2) and
water. The organic layer is separated, washed with brine solution
until pH=6, and dried over sodium sulfate. The solvent is
evaporated to give the title compound (25 g, 99%). ES/MS (m/e): 234
(M+H).
Preparation 5
1-(3-Bromophenyl)-2-(diallylamino)ethanone oxime
##STR00014##
[0047] A solution of 1-(3-bromophenyl)-2-(diallylamino)ethanone (60
g, 204.7 mmol) in ethanol (720 mL) and pyridine (24.8 mL, 307 mmol)
is stirred 15 minutes at 22.degree. C. Hydroxylamine hydrochloride
(17 g, 246 mmol) is added in portions to the solution over 1 hour.
The reaction is warmed to 50.degree. C. for 2 hours and then heated
to 70.degree. C. for 16 hours. The solvent is evaporated and the
residue partitioned in water (300 mL) and methyl tert-butyl ether
(300 mL). The organic layer is separated and washed with water (100
mL, 2.times.) and brine (100 mL). The organic layer is dried over
sodium sulfate, filtered, and evaporated to dryness to give the
title compound (75.5 g, 79%). ES/MS (m/e): 309 (M+1).
Preparation 6
Benzyl N-allyl-N-[2-hydroxyiminoethyl]carbamate
##STR00015##
[0049] A solution of benzyl N-allyl-N-(2-oxoethyl)carbamate (25 g,
107 mmol) in acetonitrile (150 mL) is treated with hydroxylamine
hydrochloride (9.68 g, 139 mmol) and a solution of sodium acetate
trihydrate (16 g, 117.9 mmol) in water (75 mL). The mixture is
stirred at room temperature overnight. The acetonitrile is
evaporated and the aqueous solution is extracted with ethyl
acetate. The organic layer is separated, dried over magnesium
sulfate, and concentrated under vacuum to give the title compound
(24 g, 90%). ES/MS (m/e): 249 (M+H).
Preparation 7
5-Allyl-6a-(3-bromophenyl)-3,3a,4,6-tetrahydro-1H-pyrrolo[3,4-c]isoxazole
##STR00016##
[0051] The crude 1-(3-bromophenyl)-2-(diallylamino)ethanone oxime
(75.5 g, 195.34 mmol) is dissolved in toluene (600 mL) and refluxed
for 12 hours. The solvent is evaporated in vacuo and the residue
dissolved in a mixture of aqueous 1 N HCl (1 L) and methyl
tert-butyl ether (300 mL). The mixture is stirred for 15 minutes
and diatomaceous earth (10 g) is added. The mixture is stirred for
an additional 20 minutes and filtered through diatomaceous earth.
The filter cake is washed with additional aqueous 1 N HCl (200 mL)
and methyl tert-butyl ether (200 mL). The organic layer is
separated and washed with 1 N HCl (2.times.100 mL). The aqueous
layers are combined and the pH adjusted to 9 with NaOH 50% w/w. The
aqueous mixture is extracted with methyl tert-butyl ether
(3.times.250 mL). The organic layers are combined, dried over
sodium sulfate and filtered. The filtrate is evaporated and dried
under vacuum to give a red solid (60 g). The red solid is diluted
with heptane (600 mL) and the mixture heated to reflux for 20
minutes. Charcoal (2 g) is added and the mixture is filtered
through diatomaceous earth. The filtrates are concentrated under
atmospheric pressure to adjust the final volume to 300 mL. The
solution is cooled to 22.degree. C. and stirred for 3 hours. A pale
yellow solid is collected by filtration and dried under vacuum to a
constant weight to give the title compound (40 g, 60%). ES/MS
(m/e): 309 (M+1).
Preparation 8
Benzyl 3,3a,4,6-tetrahydropyrrolo[3,4-c]isoxazole-5-carboxylate
##STR00017##
[0053] A solution of Benzyl
N-allyl-N-[2-hydroxyiminoethyl]carbamate (24 g, 96.6 mmol) in
dichloromethane (338 mL) is treated drop wise over 10 minutes with
a 5% w/w aqueous solution of sodium hypochlorite (106.08 mmol,
143.06 mL). The resultant mixture is stirred at room temperature
overnight. The reaction is quenched with a 40% aqueous solution of
sodium bisulfite (7 g). The organic layer is separated, dried over
magnesium sulfate, and concentrated under vacuum. The crude product
is purified over silica gel eluting with 5% ethyl acetate in
hexanes to give the title compound (18 g, 75%). ES/MS (m/e): 247
(M+H).
Preparation 9
Benzyl
6a-(5-bromo-2-fluoro-phenyl)-3,3a,4,6-tetrahydro-1H-pyrrolo[3,4-c]i-
soxazole-5-carboxylate
##STR00018##
[0055] A 1.6 M hexanes solution of n-butyl lithium (25.4 mL, 40.6
mmol) is added drop wise to a -78.degree. C. solution of
4-bromo-1-fluoro-2-iodobenzene (12.22 g, 40.6 mmol) in
tetrahydrofuran (60 mL) to give a yellow solution that is stirred
at -78.degree. C. for 15 minutes. Boron trifluoride etherate (5.14
mL, 40.6 mmol) is added to a separate -78.degree. C. solution of
benzyl 3,3a,4,6-tetrahydropyrrolo[3,4-c]isoxazole-5-carboxylate (5
g, 20.3 mmol) in tetrahydrofuran (60 mL) and the mixture is stirred
at -78.degree. C. for 5 minutes. This solution is added to the
previously prepared -78.degree. C. organolithium mixture via
cannula. The combined mixture is stirred for 30 minutes at
-78.degree. C. The mixture is quenched with saturated aqueous
ammonium chloride and warmed to room temperature. The mixture is
extracted with ethyl acetate (3.times.) and the organic extracts
are combined, dried over sodium sulfate, filtered and the solvent
removed in vacuo. The crude product is purified over silica gel
with a 35 minute 5% to 100% ethyl acetate in hexanes gradient to
give the title compound (2.27 g, 27%). ES/MS (m/e):
(.sup.79Br/.sup.81Br) 421/423 (M+H).
Preparation 10
Benzyl
1-(benzoylcarbamothioyl)-6a-(5-bromo-2-fluoro-phenyl)-3,3a,4,6-tetr-
ahydropyrrolo[3,4-c]isoxazole-5-carboxylate
##STR00019##
[0057] Benzoyl isothiocyanate (2.87 mL, 21.28 mmol) is added drop
wise to a solution of benzyl
6a-(5-bromo-2-fluoro-phenyl)-3,3a,4,6-tetrahydro-1H-pyrrolo[3,4-c]isoxazo-
le-5-carboxylate (5.977 g, 14.2 mmol) in tetrahydrofuran (95 mL)
and stirred overnight under nitrogen. The solvent is removed in
vacuo. The crude product is purified over silica gel with a 30
minute 5% to 100% EtOAc in hexanes gradient to give the title
compound (6.05 g, 73%). ES/MS (m/e): (.sup.79Br/.sup.81Br) 584/586
(M+H).
Preparation 11
[1-Allyl-4-amino-4-(3-bromophenyl)pyrrolidin-3-yl]methanol
##STR00020##
[0059] A 22.degree. C. solution of
5-allyl-6a-(3-bromophenyl)-3,3a,4,6-tetrahydro-1H-pyrrolo[3,4-c]isoxazole
(40 g, 129.4 mmol) in acetic acid (400 mL) is treated with zinc
dust (42.3 g, 646.8 mmol) in one portion. The reaction is stirred
vigorously at room temperature for 1 hour. Ethyl acetate (400 mL)
is added and the mixture is filtered through diatomaceous earth.
The filtrate is evaporated and the residue dried under vacuum. The
residue is partitioned in water (300 mL) and MTBE (300 mL). The pH
is adjusted to 8 with sodium hydroxide 50% w/w and the organic
layer is separated, dried over sodium sulfate, and filtered. The
filtrate is evaporated and the residue dried under vacuum to give
the title compound (41 g, 97%). ES/MS (m/e): 311 (M+1).
Preparation 12
Benzyl
3-(benzoylcarbamothioylamino)-3-(5-bromo-2-fluoro-phenyl)-4-(hydrox-
ymethyl)pyrrolidine-1-carboxylate
##STR00021##
[0061] A mixture of benzyl
1-(benzoylcarbamothioyl)-6a-(5-bromo-2-fluoro-phenyl)-3,3a,4,6-tetrahydro-
pyrrolo[3,4-c]isoxazole-5-carboxylate (6.05 g 10.4 mmol) and zinc
(dust, <10 micron) (6.77 g, 103.5 mmol) is stirred in acetic
acid (52 mL) at room temperature overnight under nitrogen. The
reaction is diluted with ethyl acetate and filtered through
diatomaceous earth. The solvent is removed in vacuo and the residue
is diluted with ethyl acetate, water and saturated aqueous sodium
bicarbonate. The mixture is extracted with ethyl acetate
(3.times.), the combined organic layers are combined and dried over
sodium sulfate, filtered and the solvent removed in vacuo. The
crude product is purified over silica gel with a 30 minute 5% to
100% EtOAc in hexanes gradient to give the title compound (5.222 g,
86%). ES/MS (m/e): (.sup.79Br/.sup.81Br) 586/588 (M+H).
Preparation 13
[(3R,4S)-1-Allyl-4-amino-4-(3-bromophenyl)pyrrolidin-3-yl]methanol;
(2R,3R)-2,3-bis[(4-methylbenzoyl)oxy]butanedioic acid
##STR00022##
[0063] A solution of
[1-allyl-4-amino-4-(3-bromophenyl)pyrrolidin-3-yl]methanol (77 g,
235 mmol) in isopropyl alcohol (914 mL) is heated to 70.degree. C.
Di-p-toluoyl-L-tartaric acid (86.2 g, 223 mmol) is added and the
mixture is cooled to 22.degree. C. over 2 hours and stirred
overnight. The slurry is filtered to collect a pale yellow solid
and washed with isopropyl alcohol. The solid is dried under vacuum
to give the title compound (63 g, 36%). ES/MS (m/e): 311 (M+1). The
product is analyzed by reverse phase chiral chromatography:
Analysis of the first eluting isomer (Column: Chiralpak ID-3
4.6.times.50 mm; eluent: 70:30, aqueous 20 mM ammonium bicarbonate:
acetonitrile; flow: 1.5 mL/min at UV 215 nm) confirms the
enantiomerically enriched (96% ee) enantiomer with R.sub.t=1.26
minutes.
Preparation 14
[(3R,4S)-1-Allyl-4-amino-4-(3-bromophenyl)pyrrolidin-3-yl]methanol
##STR00023##
[0065]
[(3R,4S)-1-Allyl-4-amino-4-(3-bromophenyl)pyrrolidin-3-yl]methanol;
(2R,3R)-2,3-bis[(4-methylbenzoyl)oxy]butanedioic acid (63 g 85.8
mmol) is combined with aqueous 1 N HCl (800 mL) and ethyl acetate
(400 mL) and the mixture is stirred for 15 minutes at 22.degree. C.
The layers are separated and the pH of the aqueous layer is
adjusted to 10 with sodium hydroxide 50% w/w. The aqueous mixture
is extracted with methyl tert-butyl ether (3.times.250 mL). The
combined organic layers are dried over magnesium sulfate, filtered
and evaporated to dryness to give the title compound (27 g, 99%).
ES/MS (m/e): 311 (M+1).
Preparation 15
N-[(4aR,7aS)-6-Allyl-7a-(3-bromophenyl)-4,4a,5,7-tetrahydropyrrolo[3,4-d][-
1,3]thiazin-2-yl]benzamide
##STR00024##
[0067] A solution of
[(3R,4S)-1-allyl-4-amino-4-(3-bromophenyl)pyrrolidin-3-yl]methanol
(27 g; 86.7 mmol) in tetrahydrofuran (270 mL) is cooled to
-5.degree. C. under a nitrogen atmosphere. Benzoyl isothiocyanate
(12.3 mL, 91 mmol) is added drop wise keeping the temperature below
0.degree. C. The reaction is allowed to warm to 22.degree. C. over
1 hour. 1,1'-Carbonyldiimidazole (28.1 g, 173.5 mmol) is added in a
single portion and the reaction is stirred for 1 hour at 22.degree.
C. and then heated to reflux for 16 hours. The solvent is removed
in vacuo and the residue dried under vacuum. The crude material is
partitioned in methyl tert-butyl ether (500 mL) and water (250 mL).
The organic layer is separated, dried over magnesium sulfate,
filtered and evaporated to dryness. The crude material is purified
over a silica gel gradient of 90/10 to 60/40 methylene
chloride/ethyl acetate to give the title compound (27 g, 68%).
ES/MS (m/e): 456 (M+1).
Preparation 16
Benzyl
2-benzamido-7a-(5-bromo-2-fluoro-phenyl)-4,4a,5,7-tetrahydropyrrolo-
[3,4-d][1,3]thiazine-6-carboxylate
##STR00025##
[0069] 1,1'-carbonyldiimidazole (2.87 g, 17.7 mmol) is added to a
solution of benzyl
3-(benzoylcarbamothioylamino)-3-(5-bromo-2-fluoro-phenyl)-4-(hy-
droxymethyl)pyrrolidine-1-carboxylate (5.198 g, 8.86 mmol) in
tetrahydrofuran (52 mL). The mixture is stirred for 1.5 hours at
room temperature and then the reaction is heated at reflux
overnight under nitrogen. The reaction is cooled, diluted with
water, and extracted with ethyl acetate (3.times.). The organic
layers are combined, dried over sodium sulfate, filtered, and the
solvent removed in vacuo. The crude product is purified over silica
gel with a 30 minute 5% to 100% EtOAc in hexanes gradient to give
the title compound (2.93 g, 58%). ES/MS (m/e):
(.sup.79Br/.sup.81Br). 568/570 (M+H)
Preparation 17
N-[(4aR,7aS)-7a-(3-Bromophenyl)-4a,5,6,7-tetrahydro-4H-pyrrolo[3,4-d][1,3]-
thiazin-2-yl]benzamide
##STR00026##
[0071] A room temperature mixture of
N-[(4aR,7aS)-6-allyl-7a-(3-bromophenyl)-4,4a,5,7-tetrahydropyrrolo[3,4-d]-
[1,3]thiazin-2-yl]benzamide (1 g, 2.19 mmol) and
N,N-dimethylbarbituric acid (0.868 g, 5.48 mmol) in chloroform (22
mL) is degassed by bubbling nitrogen through the resulting slurry
at RT for 5 min. The mixture is treated with
tetrakis(triphenylphosphine)palladium (0.261 g, 219 .mu.moles) and
is stirred for 1.5 hours under nitrogen.
[0072] In a separate flask, a mixture of
N-[(4aR,7aS)-6-allyl-7a-(3-bromophenyl)-4,4a,5,7-tetrahydropyrrolo[3,4-d]-
[1,3]thiazin-2-yl]benzamide (22.2 g, 48.6 mmol) and
N,N-dimethylbarbituric acid (19.28 g, 121.6 mmol) in chloroform
(486 mL) is degassed by bubbling nitrogen through the resulting
slurry at RT for 5 min. The mixture is treated with
tetrakis(triphenylphosphine)palladium (5.79 g, 4.86 mmol) and is
stirred for 2 hours under nitrogen.
[0073] The two reactions are combined and the solvent is removed in
vacuo to give the crude product. The crude material is purified
over silica gel with a 30 minute 0.5% to 10% methanol in
dichloromethane gradient to give the title compound (22.4 g, 100%).
ES/MS (m/e): (.sup.79Br/.sup.81Br) 416/418 (M+H).
Preparation 18
N-[7a-(5-Bromo-2-fluoro-phenyl)-4a,5,6,7-tetrahydro-4H-pyrrolo[3,4-d][1,3]-
thiazin-2-yl]benzamide
##STR00027##
[0075] Iodotrimethylsilane (2.21 mL, 15.46 mmol) is added drop wise
to a room temperature solution of benzyl
2-benzamido-7a-(5-bromo-2-fluoro-phenyl)-4,4a,5,7-tetrahydropyrrolo[3,4-d-
][1,3]thiazine-6-carboxylate (2.93 g, 5.15 mmol) in acetonitrile
(44 mL). The reaction is stirred at room temperature for two hours
and the solvent is removed in vacuo. The crude product is purified
with an SCX column using 3:1 dichloromethane:methanol and then 2:1
dichloromethane:7 N ammonia in methanol to give the title compound
(2.098 g, 94%). ES/MS (m/e): (.sup.79Br/.sup.81Br) 434/436
(M+H).
Preparation 19
tert-Butyl
(4aR,7aS)-2-benzamido-7a-(3-bromophenyl)-4,4a,5,7-tetrahydropyr-
rolo[3,4-d][1,3]thiazine-6-carboxylate
##STR00028##
[0077] A room temperature solution of
N-[(4aR,7aS)-7a-(3-bromophenyl)-4a,5,6,7-tetrahydro-4H-pyrrolo[3,4-d][1,3-
]thiazin-2-yl]benzamide (22.4 g, 36.69 mmol) in dichloromethane
(367 mL) is treated with di-t-butyldicarbonate (8.81 g, 40.36 mmol)
followed by triethylamine (7.67 mL, 55.04 mmol) and the reaction is
stirred at room temperature for 1 hour under nitrogen. The solvent
is removed in vacuo and the crude product is purified over silica
gel with a 25 minute 5% to 100% ethyl acetate in hexanes gradient
to give the title compound (20.22 g, 100%). ES/MS (m/e):
(.sup.79Br/.sup.81Br) 516/518 (M+H).
Preparation 20
tert-Butyl
2-benzamido-7a-(5-bromo-2-fluoro-phenyl)-4,4a,5,7-tetrahydropyr-
rolo[3,4-d][1,3]thiazine-6-carboxylate
##STR00029##
[0079] Di-t-butyldicarbonate (1.16 g, 5.31 mmol) and triethylamine
(1.01 mL, 7.25 mmol) are added to a solution of
N-[7a-(5-bromo-2-fluoro-phenyl)-4a,5,6,7-tetrahydro-4H-pyrrolo[3,4-d][1,3-
]thiazin-2-yl]benzamide (2.098 g, 4.83 mmol) in dichloromethane (48
mL). The reaction is stirred for 1 hour at room temperature under
nitrogen. The solvent is removed in vacuo and the crude product is
purified over silica gel with a 30 minute 5% to 100% EtOAc in
hexanes gradient to give the title compound (2.556 g, 99%). ES/MS
(m/e): (.sup.79Br/.sup.81Br) 534/536 (M+H).
Preparation 21
tert-Butyl
(4aR,7aS)-7a-(3-aminophenyl)-2-benzamido-4,4a,5,7-tetrahydropyr-
rolo[3,4-d][1,3]thiazine-6-carboxylate
##STR00030##
[0081] A solution of tert-butyl
(4aR,7aS)-2-benzamido-7a-(3-bromophenyl)-4,4a,5,7-tetrahydropyrrolo[3,4-d-
][1,3]thiazine-6-carboxylate (5 g, 9.7 mmol) and
trans-N,N'-dimethyl-1,2-cyclohexanediamine (220.3 mg, 1.5 mmol) in
ethanol (100 mL) is treated with sodium azide (1.30 g, 19.4 mmol).
An aqueous solution of L-ascorbic acid sodium salt (0.66 M, 3.2 mL,
2.1 mmol) and water (10 mL) is added and the top of the flask is
purged with nitrogen. The mixture is treated with an aqueous
solution of copper(II)sulfate pentahydrate (0.33 M, 3.2 mL, 1.1
mmol) and the mixture is immediately heated on a preheated hot
plate at 80.degree. C. for 1.5 hrs under nitrogen. A homogeneous
mixture is obtained upon heating. The reaction is cooled and ice
water is added. The mixture is extracted with ethyl acetate
(3.times.). The organic layers are combined and dried over sodium
sulfate, filtered, and the solvent is removed in vacuo to give
crude azide product. The crude azide product is combined with 10%
palladium on carbon (2 g) in cold ethanol (150 mL) and the mixture
is purged using vacuum/nitrogen and then vacuum/hydrogen. The
mixture is stirred at room temperature under 30 psi of hydrogen for
2 hours. The reaction is vented and the mixture is filtered through
diatomaceous earth using dichloromethane to rinse the filter cake.
The solvent is removed from the filtrate in vacuo and the crude
product is purified over silica gel with 50% ethyl acetate in
dichloromethane to give the title compound (4 g, 91%). ES/MS (m/e):
453 (M+H).
Preparation 22
tert-Butyl
7a-(5-amino-2-fluoro-phenyl)-2-benzamido-4,4a,5,7-tetrahydropyr-
rolo[3,4-d][1,3]thiazine-6-carboxylate
##STR00031##
[0083] A solution of tert-butyl
2-benzamido-7a-(5-bromo-2-fluoro-phenyl)-4,4a,5,7-tetrahydropyrrolo[3,4-d-
][1,3]thiazine-6-carboxylate (2.556 g, 4.8 mmol) and
trans-N,N'-dimethyl-1,2-cyclohexanediamine (150 mg, 1.1 mmol) in
ethanol (50 mL) is treated with sodium azide (933 mg, 14.3 mmol).
An aqueous solution of L-ascorbic acid sodium salt (0.66 M, 3.2 mL,
2.1 mmol) and water (1 mL) are added and the top of the flask is
purged with nitrogen. The mixture is treated with an aqueous
solution of copper(II)sulfate pentahydrate (0.33 M, 3.2 mL, 1.1
mmol) and the mixture is immediately heated on a preheated hot
plate at 80.degree. C. for 1.5 hrs under nitrogen. A homogeneous
mixture is obtained upon heating. The reaction is cooled, diluted
with ice water, and the mixture is extracted with ethyl acetate
(3.times.). The organic layers are combined and dried over sodium
sulfate, filtered, and the solvent removed in vacuo to give the
crude azide product. The crude azide product is combined with 10%
palladium on carbon (1 g) in cold ethanol (150 mL) and the mixture
is purged using vacuum/nitrogen and then vacuum/hydrogen. The
mixture is stirred at room temperature under 30 psi of hydrogen for
5 hours. The reaction is vented, filtered through diatomaceous
earth, and the filter cake rinsed with dichloromethane. Remove the
solvent from the filtrate in vacuo and purify the crude product
over silica gel with 50% ethyl acetate in dichloromethane to afford
the titled compound (2.014 g, 89%). ES/MS (m/e): 471 (M+H).
Preparation 23
tert-Butyl
(4aR,7aS)-2-benzamido-7a-[3-[(5-fluoropyridine-2-carbonyl)amino-
]phenyl]-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazine-6-carboxylate
##STR00032##
[0085] A slurry of tert-butyl
(4aR,7aS)-7a-(3-aminophenyl)-2-benzamido-4,4a,5,7-tetrahydropyrrolo[3,4-d-
][1,3]thiazine-6-carboxylate (93 mg, 0.21 mmol),
5-fluoropyridine-2-carboxylic acid (31.9 mg, 0.23 mmol),
1-hydroxybenzotriazole hydrate (56.7 mg, 0.41 mmol) and
1-(2-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (40 mg,
0.21 mmol) in dichloromethane (4 mL) containing dimethylformamide
(1 ml) is treated with diisopropylethylamine (179.2 .mu.L, 1.03
mmol) and the resulting mixture is stirred at room temperature
overnight. The reaction mixture is diluted with dichloromethane (5
mL) and saturated aqueous sodium bicarbonate (15 mL). The organic
layer is separated and washed with saturated aqueous sodium
chloride (10 mL), dried over sodium sulfate, filtered, and the
solvent removed in vacuo to give the crude title compound (105 mg,
89%). ES/MS (m/e): 576 (M+H).
Preparation 24
N-[3-[(4aR,7aS)-2-Benzamido-4a,5,6,7-tetrahydro-4H-pyrrolo[3,4-d][1,3]thia-
zin-7a-yl]phenyl]-5-fluoro-pyridine-2-carboxamide;
2,2,2-trifluoroacetic acid
##STR00033##
[0087] tert-Butyl
(4aR,7aS)-2-benzamido-7a-[3-[(5-fluoropyridine-2-carbonyl)amino]phenyl]-4-
,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazine-6-carboxylate (105
mg, 0.18 mmol) is dissolved in dichloromethane (2 mL) and treated
with trifluoroacetic acid (500 .mu.L, 6.6 mmol). The resulting
yellow solution is stirred for 4 hours at room temperature and the
solvent removed in vacuo to give the crude title product (190 mg,
100%). ES/MS (m/e): 476 (M+H).
Preparation 25
N-[(4aR,7aS)-7a-(3-Aminophenyl)-4a,5,6,7-tetrahydro-4H-pyrrolo[3,4-d][1,3]-
thiazin-2-yl]benzamide
##STR00034##
[0089] Trifluoroacetic acid (25 mL) is added to a solution of
tert-butyl
(4aR,7aS)-7a-(3-aminophenyl)-2-benzamido-4,4a,5,7-tetrahydropyrrolo[3,4-d-
][1,3]thiazine-6-carboxylate (4 g, 8.84 mmol) in dichloromethane
(100 mL) and the mixture is stirred at room temperature under
nitrogen for 4 hours. The solvent is removed in vacuo and the crude
product is purified with an SCX column using 3:1
dichloromethane:methanol and then 2:1 dichloromethane:7 N ammonia
in methanol to give the title compound (2.49 g, 80%). ES/MS (m/e):
353 (M+H).
Preparation 26
N-[7a-(5-Amino-2-fluoro-phenyl)-4a,5,6,7-tetrahydro-4H-pyrrolo[3,4-d][1,3]-
thiazin-2-yl]benzamide
##STR00035##
[0091] Trifluoroacetic acid (10 mL) is added to a solution of
tert-butyl
7a-(5-amino-2-fluoro-phenyl)-2-benzamido-4,4a,5,7-tetrahydropyrrolo[3,4-d-
][1,3]thiazine-6-carboxylate (2.013 g, 4.28 mmol) in
dichloromethane (30 mL) and the mixture is stirred at room
temperature under nitrogen for 4 hours. The solvent removed in
vacuo and the crude product is purified with an SCX column using
3:1 dichloromethane:methanol and then 2:1 dichloromethane:7 N
ammonia in methanol to give the title compound (1.555 g, 98%).
ES/MS (m/e): 371 (M+H).
Preparation 27
N-[(4aR,7aS)-7a-(3-Aminophenyl)-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrah-
ydropyrrolo[3,4-d][1,3]thiazin-2-yl]benzamide
##STR00036##
[0093] A solution of
N-[(4aR,7aS)-7a-(3-aminophenyl)-4a,5,6,7-tetrahydro-4H-pyrrolo[3,4-d][1,3-
]thiazin-2-yl]benzamide (2.49 g, 7.06 mmol),
5-fluoro-2-chloropyrimidine (3.74 g, 28.26 mmol), and
diisopropylethylamine (6.16 mL, 35.32 mmol) in 1,4-dioxane (60 mL)
is heated to reflux for 4 hours under nitrogen. The reaction is
cooled, diluted with water and extracted with ethyl acetate
(3.times.). The combined organic extracts are dried over sodium
sulfate, filtered and the solvent is removed in vacuo to give the
crude product. The crude product is purified over silica gel with a
25 minute 5% to 100% ethyl acetate in hexanes gradient to give the
title compound (2.51 g, 79%). ES/MS (m/e): 449 (M+H).
Preparation 28
N-[3-[(4aR,7aS)-2-Benzamido-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydro-
pyrrolo[3,4-d][1,3]thiazin-7a-yl]phenyl]-5-fluoro-pyridine-2-carboxamide
##STR00037##
[0095] A solution of
N-[3-[(4aR,7aS)-2-benzamido-4a,5,6,7-tetrahydro-4H-pyrrolo[3,4-d][1,3]thi-
azin-7a-yl]phenyl]-5-fluoro-pyridine-2-carboxamide;
2,2,2-trifluoroacetic acid (150 mg, 254 .mu.mol),
5-fluoro-2-chloropyrimidine (68 mg, 51 .mu.mol) and
diisopropylethylamine (98 .mu.L, 56 .mu.mol) is heated in dimethyl
sulfoxide (5 mL) overnight at 40.degree. C. Additional
5-fluoro-2-chloropyrimidine (68 mg, 51 .mu.mol) and
diisopropylethylamine (98 .mu.L, 56 .mu.mol) is added and the
mixture is heated overnight at 50.degree. C. Additional
5-fluoro-2-chloropyrimidine (68 mg, 51 .mu.mol) and
diisopropylethylamine (98 .mu.L, 56 .mu.mol) is added and the
mixture is heated overnight at 50.degree. C. for a third night. The
reaction is cooled, diluted with saturated aqueous sodium carbonate
(50 mL) to give a slurry that is filtered and dried in a vacuum
oven at 50.degree. C. for 4 hours to give the title compound (60
mg, 41%). ES/MS (m/e): 449 (M+H).
Alternate Preparation 28
[0096]
N-[(4aR,7aS)-7a-(3-Aminophenyl)-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-
-tetrahydropyrrolo[3,4-d][1,3]thiazin-2-yl]benzamide (282 mg,
628.73 .mu.mol) and 5-fluoropyridine-2-carboxylic acid (106.46 mg,
754.47 .mu.mol) are combined in dichloromethane (3 mL) and
dimethylformamide (0.5 mL). 1-Hydroxybenzotriazole (112.70 mg,
817.35 .mu.mol) and then
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (159.07
mg, 817.35 .mu.mol) is added and the resulting mixture is stirred
for 5 hours at room temperature under nitrogen. The reaction
mixture is diluted with water and the pH is adjusted with 1 N NaOH
to .about.12. The mixture is extracted with ethyl acetate
(3.times.). The organic extracts are combined, dried over sodium
sulfate, filtered and the solvent removed in vacuo to give the
crude product. The crude product is purified over silica gel with a
20 minute 5% to 100% ethyl acetate in hexanes gradient to give the
title compound (327 mg, 91%). ES/MS (m/e): 571 (M+H).
Preparation 29
N-[7a-(5-Amino-2-fluoro-phenyl)-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrah-
ydropyrrolo[3,4-d][1,3]thiazin-2-yl]benzamide
##STR00038##
[0098] A solution of
N-[7a-(5-amino-2-fluoro-phenyl)-4a,5,6,7-tetrahydro-4H-pyrrolo[3,4-d][1,3-
]thiazin-2-yl]benzamide (705 mg, 1.90 mmol),
5-fluoro-2-chloropyrimidine (1.01 g, 7.61 mmol), and
diisopropylethylamine (1.66 mL, 9.52 mmol) are heated in
1,4-dioxane (20 mL) to reflux for 4 hours under nitrogen. The
reaction is cooled, diluted with water, and extracted with ethyl
acetate (3.times.). The organic layers are combined, dried over
sodium sulfate, filtered and the solvent removed in vacuo to give
crude product. The crude product is purified over silica gel with a
25 minute 5% to 100% ethyl acetate in hexanes gradient to give the
title compound (590 mg, 66%). ES/MS (m/e): 467 (M+H).
Preparation 30
N-[3-[(4aR,7aS)-2-Benzamido-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydro-
pyrrolo[3,4-d][1,3]thiazin-7a-yl]phenyl]-5-methoxy-pyrazine-2-carboxamide
##STR00039##
[0100]
N-[(4aR,7aS)-7a-(3-Aminophenyl)-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-
-tetrahydropyrrolo[3,4-d][1,3]thiazin-2-yl]benzamide (400 mg,
891.81 .mu.mole) and 5-methoxypyrazine-2-carboxylic acid (165 mg,
1.07 mmol) are combined in dichloromethane (4 mL) and
dimethylformamide (0.5 mL). 1-Hydroxybenzotriazole (160 mg, 1.16
mmol) and then 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide
hydrochloride (226 mg, 1.16 mmol) are added and the resulting
mixture is stirred for 5 hours at room temperature under nitrogen.
The reaction mixture is diluted with water and the pH is adjusted
to .about.12 with 1 N NaOH. The mixture is extracted with ethyl
acetate (3.times.). The combined organic extracts are dried over
sodium sulfate, filtered and the solvent removed in vacuo. The
crude product is purified over silica gel with a 20 minute 5% to
100% ethyl acetate in hexanes gradient to give the title compound
(482 mg, 92%). ES/MS (m/e): 585 (M+H).
Preparation 31
N-[3-[2-Benzamido-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrrolo[3,-
4-d][1,3]thiazin-7a-yl]-4-fluoro-phenyl]-5-fluoro-pyridine-2-carboxamide
##STR00040##
[0102]
N-[7a-(5-Amino-2-fluoro-phenyl)-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-
-tetrahydropyrrolo[3,4-d][1,3]thiazin-2-yl]benzamide (302 mg, 647
.mu.mol) and 5-fluoropyridine-2-carboxylic acid (110 mg, 777
.mu.mol) are combined in dichloromethane (3 mL) and
dimethylformamide (0.5 mL). 1-Hydroxybenzotriazole (116 mg, 842
.mu.mol) and then 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide
hydrochloride (164 mg, 842 .mu.mol) are added and the mixture is
stirred overnight at room temperature under nitrogen. The reaction
mixture is diluted with water and the pH adjusted with 1 N NaOH to
-12 and then extracted with ethyl acetate (3.times.). The organic
layers are combined and filtered to collect the insoluble material.
The solids are washed with water and ethyl acetate and dried under
vacuum to give the title compound. The organic layer from the
filtrate is dried over sodium sulfate, filtered and the solvent
removed in vacuo. The residue is purified over silica gel with a 20
minute 5% to 100% ethyl acetate in hexanes gradient to give
additional title compound with a combined yield (275 mg, 72%).
ES/MS (m/e): 590 (M+H).
Preparation 32
N-[(4aR,7aS)-7a-(5-Amino-2-fluoro-phenyl)-6-(5-fluoropyrimidin-2-yl)-4,4a,-
5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-2-yl]benzamide, (isomer
1)
##STR00041##
[0104] Racemic
N-[7a-(5-amino-2-fluoro-phenyl)-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetra-
hydropyrrolo[3,4-d][1,3]thiazin-2-yl]benzamide (1.694 g, 3.63 mmol)
is chirally purified by HPLC (Column: Chiralcel OJ, 8.times.35 cm;
eluent: 90% methanol (0.2% dimethylethylamine) and 10%
acetonitrile; flow 400 mL/min at UV 280 nm). Analysis of the first
eluting isomer (Column: Chiralcel OJ-H 0.46.times.15 cm; eluent:
10:90 acetonitrile:methanol (with 0.2% dimethylethylamine); flow:
0.6 mL/min at UV 280 nm) confirms the enantiomerically enriched
(99% ee) enantiomer with R.sub.t=6.70 minutes, (723 mg, 43%). ES/MS
(m/e): 467 (M+H).
Preparation 33
N-[3-[(4aR,7aS)-2-Benzamido-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydro-
pyrrolo[3,4-d][1,3]thiazin-7a-yl]-4-fluoro-phenyl]-5-methoxy-pyrazine-2-ca-
rboxamide, (isomer 1)
##STR00042##
[0106]
N-[(4aR,7aS)-7a-(5-Amino-2-fluoro-phenyl)-6-(5-fluoropyrimidin-2-yl-
)-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-2-yl]benzamide
(0.361 g, 0.77 mmol, isomer 1) is dissolved in a mixture of
dichloromethane (4 mL) and DMF (0.5 mL).
5-Methoxypyrazine-2-carboxylic acid (240 mg, 1.55 mmol),
1-hydroxybenzotriazole (210 mg, 1.55 mmol) and
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (300
mg, 1.55 mmol) are added to the mixture and the mixture is stirred
overnight at room temperature. The reaction solution is added
directly onto a 12 g silica gel loading column and purified using a
40 g silica gel column and eluting with a 0-100% ethyl
acetate/hexanes gradient. The product is dissolved in ethyl acetate
(200 mL), washed with 1 N NaOH (2.times.50 mL), and with brine
(1.times.50 mL). The silica gel purification is repeated as
described above to give the title compound (350 mg, 74%). ES/MS
(m/e): 603 (M+H).
Preparation 34
N-[3-[(4aR,7aS)-2-Benzamido-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydro-
pyrrolo[3,4-d][1,3]thiazin-7a-yl]phenyl]-5-cyano-pyridine-2-carboxamide
##STR00043##
[0108]
N-[(4aR,7aS)-7a-(3-Aminophenyl)-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-
-tetrahydropyrrolo[3,4-d][1,3]thiazin-2-yl]benzamide (0.30 g, 0.67
mmol) is dissolved in dichloromethane (10 mL) and
5-cyanopyridine-2-carboxylic acid (129 mg, 0.87 mmol),
1-hydroxybenzotriazole (185 mg, 1.34 mmol) and
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (169
mg, 0.87 mmol) are added. Diisopropylethyamine (0.35 mL, 2 mmol) is
added and the reaction is stirred at room temperature overnight.
The material is purified directly with silica gel chromatography
eluting with a 0-100% ethyl acetate/hexanes gradient to give the
title compound (360 mg, 88%). ES/MS (m/e): 579 (M+H).
Preparation 35
N-[3-[(4aR,7aS)-2-Benzamido-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydro-
pyrrolo[3,4-d][1,3]thiazin-7a-yl]phenyl]-3,5-difluoro-pyridine-2-carboxami-
de
##STR00044##
[0110]
N-[(4aR,7aS)-7a-(3-Aminophenyl)-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-
-tetrahydropyrrolo[3,4-d][1,3]thiazin-2-yl]benzamide (0.30 g, 0.67
mmol) is dissolved in dichloromethane (10 mL) and
3,5-difluoropyridine-2-carboxylic acid (138 mg, 0.87 mmol),
1-hydroxybenzotriazole (185 mg, 1.34 mmol) and
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (169
mg, 0.87 mmol) are added. Diisopropylethylamine (0.35 mL, 2 mmol)
is added and the reaction is stirred at room temperature overnight.
The reaction is purified directly with silica gel chromatography
eluting with a 0-100% ethyl acetate/hexanes gradient to give the
title compound (330 mg, 84%). ES/MS (m/e): 590 (M+H).
Preparation 36
N-[3-[(4aR,7aS)-2-Benzamido-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydro-
pyrrolo[3,4-d][1,3]thiazin-7a-yl]-4-fluoro-phenyl]-5-cyano-pyridine-2-carb-
oxamide, (isomer 1)
##STR00045##
[0112]
N-[(4aR,7aS)-7a-(5-Amino-2-fluoro-phenyl)-6-(5-fluoropyrimidin-2-yl-
)-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-2-yl]benzamide
(0.180 g, 0.39 mmol, isomer 1) is dissolved in a mixture of
dichloromethane (2 mL) and DMF (0.25 mL).
5-Cyanopyridine-2-carboxylic acid (114 mg, 0.77 mmol),
1-hydroxybenzotriazole (106 mg, 0.77 mmol) and
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (150
mg, 0.77 mmol) are added and the reaction is stirred at room
temperature overnight. The mixture is diluted with water (10 mL),
ethyl acetate (10 mL) and added to a solution of 1 N NaOH (100 mL).
The mixture is extracted with EtOAc (2.times.100 mL) and the
organic layers are combined and washed with brine. The organic
layer is dried over MgSO.sub.4, filtered and concentrated. The
residue is purified over silica gel chromatography using a 0-100%
ethyl acetate/hexanes gradient to give the title compound (133 mg,
57%). ES/MS (m/e): 597 (M+H).
Preparation 37
N-[3-[(4aR,7aS)-2-Benzamido-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydro-
pyrrolo[3,4-d][1,3]thiazin-7a-yl]-4-fluoro-phenyl]-3,5-difluoro-pyridine-2-
-carboxamide, (isomer 1)
##STR00046##
[0114]
N-[(4aR,7aS)-7a-(5-Amino-2-fluoro-phenyl)-6-(5-fluoropyrimidin-2-yl-
)-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-2-yl]benzamide
(0.180 g, 0.39 mmol, isomer 1) is dissolved in a mixture of
dichloromethane (2 mL) and DMF (0.25 mL).
5-Cyanopyridine-2-carboxylic acid (114 mg, 0.77 mmol),
1-hydroxybenzotriazole (106 mg, 0.77 mmol) and
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (150
mg, 0.77 mmol) are added and the reaction is stirred at room
temperature overnight. The mixture is diluted with water (10 mL)
and ethyl acetate (10 mL) and then poured into a solution of 1 N
NaOH (100 mL). The mixture is extracted with EtOAc (2.times.100 mL)
the organic extracts are combined and washed with brine. The
organic layers are dried over MgSO.sub.4, filtered and
concentrated. The residue is purified via silica gel chromatography
using a 0-100% ethyl acetate/hexanes gradient to give the title
compound (190 mg, 80%). ES/MS (m/e): 608 (M+H).
EXAMPLE A
N-[3-[2-Amino-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrrolo[3,4-d]-
[1,3]thiazin-7a-yl]-4-fluoro-phenyl]-5-fluoro-pyridine-2-carboxamide
##STR00047##
[0116] A mixture of
N-[3-[2-benzamido-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrrolo[3-
,4-d][1,3]thiazin-7a-yl]-4-fluoro-phenyl]-5-fluoro-pyridine-2-carboxamide
(293 mg, 497 .mu.mol), O-methylhydroxylamine hydrochloride (430 mg,
4.97 mmol) and pyridine (402 .mu.L, 4.97 mmol) is heated in ethanol
(13 mL) to 70.degree. C. in a capped flask for 2.5 hours. Dimethyl
sulfoxide (3 mL) is added and the mixture is heated at 70.degree.
C. overnight. Additional dimethyl sulfoxide (10 mL) is added and
heating continued at 70.degree. C. for 4 hours. Additional
O-methylhydroxylamine hydrochloride (208 mg, 2.48 mmol) and
pyridine (201 .mu.L, 2.48 mmol) is added and the mixture is heated
to 60.degree. C. for 3 hours and the mixture is stirred for 3 days
at room temperature. In a separate flask, a mixture of
N-[3-[2-benzamido-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrrolo[3-
,4-d][1,3]thiazin-7a-yl]-4-fluoro-phenyl]-5-fluoro-pyridine-2-carboxamide
(276 mg, 468 .mu.mol), O-methylhydroxylamine hydrochloride (405 mg,
4.68 mmol) and pyridine (478 .mu.L, 4.68 mmol) is heated in ethanol
(15 mL) and dimethyl sulfoxide (4 mL) at 70.degree. C. in a capped
flask overnight. Additional dimethyl sulfoxide (10 mL) is added and
heating is continued at 70.degree. C. for 4 hours. Additional
O-methylhydroxylamine hydrochloride (195 mg, 2.34 mmol) and
pyridine (189 .mu.L, 2.34 mmol) is added and heating continued at
70.degree. C. for 3 hours followed by stirring the mixture for 3
days at room temperature. The two reaction mixtures are combined
and most of the solvent removed in vacuo. The crude product is
purified on a SCX column using 3:1 dichloromethane:methanol and
then 2:1 dichloromethane:7 N ammonia in methanol. The crude product
is further purified over silica gel with a 20 minute 0.5% to 10%
gradient of 7 N ammonia methanol in dichloromethane gradient to
give the title compound (451 mg, 96%). ES/MS (m/e): 486 (M+H).
EXAMPLE 1
N-{3-[(4aR,7aS)-2-Amino-6-(5-fluoropyrimidin-2-yl)-4a,5,6,7-tetrahydropyrr-
olo[3,4-d][1,3]thiazin-7a(4H)-yl]phenyl}-5-fluoropyridine-2-carboxamide
hydrochloride
##STR00048##
[0118] A mixture of
N-[3-[(4aR,7aS)-2-benzamido-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydr-
opyrrolo[3,4-d][1,3]thiazin-7a-yl]phenyl]-5-fluoro-pyridine-2-carboxamide
(320 mg, 560 .mu.mol), O-methylhydroxylamine hydrochloride (485 mg,
5.60 mmol) and pyridine (453 .mu.L, 5.60 mmol) in ethanol (15 mL)
is heated at 65.degree. C. in a capped vial for five hours. The
reaction is cooled and the solvent removed in vacuo. The crude
product is purified over silica gel with a 30 minute 0.5% to 10%
gradient of 7 N ammonia in methanol dichloromethane gradient to
give
N-[3-[(4aR,7aS)-2-amino-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyr-
rolo[3,4-d][1,3]thiazin-7a-yl]phenyl]-5-fluoro-pyridine-2-carboxamide
(219 mg, 84%). This material is dissolved in dichloromethane (1 mL)
and methanol (0.5 mL) and 1 M hydrogen chloride in diethyl ether
(0.47 mL, 470 .mu.mol) is added. The solvent is removed in vacuo to
give the title compound (228 mg, 81%). ES/MS (m/e): 468 (M+H).
EXAMPLE 2
N-{3-[(4aR,7aS)-2-Amino-6-(5-fluoropyrimidin-2-yl)-4a,5,6,7-tetrahydropyrr-
olo[3,4-d][1,3]thiazin-7a(4H)-yl]phenyl}-5-methoxypyrazine-2-carboxamide
hydrochloride
##STR00049##
[0120] A mixture of
N-[3-[(4aR,7aS)-2-benzamido-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydr-
opyrrolo[3,4-d][1,3]thiazin-7a-yl]phenyl]-5-methoxy-pyrazine-2-carboxamide
(479 mg, 819 .mu.mol), O-methylhydroxylamine hydrochloride (709 mg,
8.19 mmol) and pyridine (663 .mu.L, 8.19 mmol) in ethanol (20 mL)
is heated at 50.degree. C. in a capped flask overnight. Dimethyl
sulfoxide (4 mL) is added and the mixture is heated to 70.degree.
C. for 4 hours to obtain a solution. The reaction is cooled and
most of the solvent is removed in vacuo. Water is added and the pH
is adjusted to .about.12 with 1 N sodium hydroxide. The mixture is
extracted with ethyl acetate (5.times.). The combined organic
extracts are dried over sodium sulfate, filtered and the solvent
removed in vacuo. The crude product is purified over silica gel
with a 30 minute 0.5% to 10% gradient of 7 N ammonia methanol in
dichloromethane gradient. The mixture is purified again on a SCX
column using 3:1 dichloromethane:methanol and then 2:1
dichloromethane:7 N ammonia in methanol to remove residual dimethyl
sulfoxide. The mixture is purified a final time over silica gel
with a 20 minute 0.5% to 10% gradient of 7 N ammonia methanol in
dichloromethane to give
N-[3-[(4aR,7aS)-2-amino-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyr-
rolo[3,4-d][1,3]thiazin-7a-yl]phenyl]-5-methoxy-pyrazine-2-carboxamide.
This material is dissolved in dichloromethane (1 mL) and methanol
(0.5 mL) and 1 M hydrogen chloride in diethyl ether (0.66 mL, 660
.mu.mol) is added. The solvent is removed in vacuo to give the
title compound (329 mg, 78%). ES/MS (m/e): 481 (M+H).
EXAMPLE 3
N-[3-[(4aR,7aS)-2-Amino-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrr-
olo[3,4-d][1,3]thiazin-7a-yl]-4-fluoro-phenyl]-5-fluoro-pyridine-2-carboxa-
mide hydrochloride
##STR00050##
[0122] Racemic
N-[3-[2-amino-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrrolo[3,4-d-
][1,3]thiazin-7a-yl]-4-fluoro-phenyl]-5-fluoro-pyridine-2-carboxamide
(451 mg, 929 .mu.mol) is chirally purified by SFC (Column:
Chiralcel OD-H (5 um), 2.1.times.25 cm; eluent: 40% methanol (0.2%
isopropylamine) in CO.sub.2; flow 70 mL/min at UV 225 nm). Chiral
analysis of the first eluting isomer: Column: Chiralcel OD-H (5
.mu.m), 4.6.times.150 mm; eluent: 40% methanol (0.2%
isopropylamine) in CO.sub.2; flow 5 mL/min at UV 225 nm confirms
the enantiomerically enriched (>99% ee) enantiomer with
R.sub.t=1.01 minutes (175 mg, 360 .mu.moles). This material (free
base, isomer 1) is dissolved in dichloromethane (1 mL) and methanol
(0.5 mL) and 1 M hydrogen chloride in diethyl ether (0.36 mL, 360
.mu.moles) is added. The solvent is removed in vacuo to give the
title compound (183 mg, 38%). ES/MS (m/e): 486 (M+H).
EXAMPLE 4
N-[3-[(4aR,7aS)-2-Amino-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrr-
olo[3,4-d][1,3]thiazin-7a-yl]-4-fluoro-phenyl]-5-methoxy-pyrazine-2-carbox-
amide hydrochloride
##STR00051##
[0124]
N-[3-[(4aR,7aS)-2-Benzamido-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tet-
rahydropyrrolo[3,4-d][1,3]thiazin-7a-yl]-4-fluoro-phenyl]-5-methoxy-pyrazi-
ne-2-carboxamide (0.350 g, 0.58 mmol, isomer 1) is dissolved in THF
(2 mL) and then methanol (4 mL) and ethanol (4 mL) are added.
O-Methylhydroxylamine hydrochloride (495 mg, 5.81 mmol) and
pyridine (470 .mu.L, 5.81 mmol) are added to the mixture and the
reaction is warmed to 50.degree. C. and stirred overnight. Silica
gel (.about.10 g) is added to the reaction and the mixture is
concentrated. The sample, dried onto silica gel, is loaded onto an
empty cartridge and purified eluting with a 0-10% gradient of 7 N
ammonia methanol in dichloromethane. The product is purified a
second time on a SCX column using 3:1 dichloromethane:methanol and
then 2:1 dichloromethane:7 N ammonia in methanol. The product is
purified a final time over silica gel with a 0% to 10% gradient of
7 N ammonia methanol in dichloromethane to give the free base of
the title compound. This material is dissolved in dichloromethane
(5 mL) and 1 M hydrogen chloride in diethyl ether (0.20 mL, 660
.mu.mol) is added. The solvent is removed in vacuo to give the
title compound (71 mg, 23%). ES/MS (m/e): 498 (M+H).
EXAMPLE 5
N-[3-[(4aR,7aS)-2-Amino-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrr-
olo[3,4-d][1,3]thiazin-7a-yl]phenyl]-5-cyano-pyridine-2-carboxamide
hydrochloride
##STR00052##
[0126]
N-[3-[(4aR,7aS)-2-Benzamido-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tet-
rahydropyrrolo[3,4-d][1,3]thiazin-7a-yl]phenyl]-5-cyano-pyridine-2-carboxa-
mide (360 mg, 0.59 mmol) is dissolved in ethanol (10 mL) and
dichloromethane (2 mL). 0-Methylhydroxylamine hydrochloride (504
mg, 5.91 mmol) and pyridine (478 .mu.L, 5.91 mmol) are added and
the reaction is stirred at room temperature over the weekend (70
hrs). The reaction is warmed to 60.degree. C. and stirred for 24
hrs. The reaction is concentrated to give the crude product and
purified via silica gel chromatography using a 0-10% gradient of 7
N ammonia methanol in dichloromethane to give the free base of the
title compound. This material is dissolved in dichloromethane (5
mL) and 1 M hydrogen chloride in diethyl ether (0.54 mL, 540
.mu.mol) is added. The solvent is removed in vacuo to give the
title compound (240 mg, 75%). ES/MS (m/e): 475 (M+H).
EXAMPLE 6
N-[3-[(4aR,7aS)-2-Amino-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrr-
olo[3,4-d][1,3]thiazin-7a-yl]phenyl]-3,5-difluoro-pyridine-2-carboxamide
hydrochloride
##STR00053##
[0128]
N-[3-[(4aR,7aS)-2-Benzamido-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tet-
rahydropyrrolo[3,4-d][1,3]thiazin-7a-yl]phenyl]-3,5-difluoro-pyridine-2-ca-
rboxamide (330 mg, 0.53 mmol) is dissolved in THF (10 mL) and
diluted with ethanol (10 mL). O-Methylhydroxylamine hydrochloride
(453 mg, 5.32 mmol) and pyridine (430 .mu.L, 5.91 mmol) are added
and the reaction is stirred at room temperature over the weekend
(70 hrs). The reaction is warmed to 60.degree. C. and stirred for
24 hrs. The mixture is concentrated onto silica gel (.about.10 g)
and purified via silica gel chromatography using a 0-10% gradient
of 7 N ammonia methanol in dichloromethane to give the free base of
the title compound. This material is dissolved in dichloromethane
(5 mL) and 1 M hydrogen chloride in diethyl ether (0.49 mL, 490
.mu.mol) is added. The solvent is removed in vacuo to give the
title compound (159 mg, 54%). ES/MS (m/e): 486(M+H).
EXAMPLE 7
N-[3-[(4aR,7aS)-2-Amino-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrr-
olo[3,4-d][1,3]thiazin-7a-yl]-4-fluoro-phenyl]-5-cyano-pyridine-2-carboxam-
ide hydrochloride
##STR00054##
[0130]
N-[3-[(4aR,7aS)-2-Benzamido-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tet-
rahydropyrrolo[3,4-d][1,3]thiazin-7a-yl]-4-fluoro-phenyl]-5-cyano-pyridine-
-2-carboxamide (133 mg, 0.22 mmol, isomer 1) is dissolved in THF (1
mL) and diluted with methanol (3 mL) and ethanol (3 mL).
O-Methylhydroxylamine hydrochloride (190 mg, 2.2 mmol) and pyridine
(180 .mu.L, 2.2 mmol) are added. The reaction is warmed to
50.degree. C. and stirred overnight. The mixture is concentrated
onto silica gel (.about.10 g) and purified via silica gel
chromatography eluting with a 0-10% gradient of 7 N ammonia
methanol in dichloromethane. The material is purified a second time
on a SCX column using 3:1 dichloromethane:methanol and then 2:1
dichloromethane:7 N ammonia in methanol. The mixture is purified a
final time over silica gel with a 0% to 10% gradient of 7 N ammonia
methanol in dichloromethane to give the free base of the title
compound. This material is dissolved in dichloromethane (5 mL) and
1 M hydrogen chloride in diethyl ether (0.27 mL, 270 .mu.mol) is
added. The solvent is removed in vacuo to give the title compound
(114 mg, 97%). ES/MS (m/e): 493 (M+H).
EXAMPLE 8
N-[3-[(4aR,7aS)-2-Amino-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrr-
olo[3,4-d][1,3]thiazin-7a-yl]-4-fluoro-phenyl]-3,5-difluoro-pyridine-2-car-
boxamide hydrochloride
##STR00055##
[0132]
N-[3-[(4aR,7aS)-2-benzamido-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tet-
rahydropyrrolo[3,4-d][1,3]thiazin-7a-yl]-4-fluoro-phenyl]-3,5-difluoro-pyr-
idine-2-carboxamide (190 mg, 0.31 mmol, isomer 1) is dissolved in
THF (1 mL) and diluted with methanol (3 mL) and ethanol (3 mL).
O-Methylhydroxylamine hydrochloride (267 mg, 3.1 mmol) and pyridine
(253 .mu.L, 3.1 mmol) are added and the reaction is warmed to
50.degree. C. and stirred overnight. The reaction is purified on an
SCX column using 3:1 dichloromethane:methanol and then 2:1
dichloromethane:7 N ammonia in methanol. The material is purified a
final time over silica gel with a 0% to 10% gradient of 7 N ammonia
methanol in dichloromethane to give the free base of the title
compound. This material is dissolved in dichloromethane (5 mL) and
1 M hydrogen chloride in diethyl ether (0.20 mL, 200 .mu.mol) is
added. The solvent is removed in vacuo to give the title compound
(101 mg, 60%). ES/MS (m/e): 504 (M+H).
In Vitro Assay Procedures:
[0133] For in vitro enzymatic and cellular assays, test compounds
are prepared in DMSO to make up a 10 mM stock solution. The stock
solution is serially diluted in DMSO to obtain a ten-point dilution
curve with final compound concentrations ranging from 10 mM to 0.05
nM in a 96-well round-bottom plate before conducting the in vitro
enzymatic and whole cell assays.
In Vitro Protease Inhibition Assays
Expression of Human BACE1
[0134] Human BACE1 (accession number: AF190725) is cloned from
total brain cDNA by RT-PCR. The nucleotide sequences corresponding
to amino acid sequences #1 to 460 are inserted into the cDNA
encoding human IgG.sub.1 (Fc) polypeptide (Vassar et al. 1999).
This fusion protein of BACE1(1-460) and human Fc, named huBACE1:Fc,
is constructed into the pJB02 vector. Human BACE1(1-460):Fc
(huBACE1:Fc) is transiently expressed in HEK293 cells. 250 .mu.g
cDNA of each construct is mixed with Fugene 6 and added to 1 liter
HEK293 cells. Four days after the transfection, conditioned media
are harvested for purification.
Purification of huBACE1:Fc
[0135] huBACE1:Fc is purified by Protein A chromatography. The
enzyme is stored at -80.degree. C. in small aliquots.
BACE1 FRET Assay
[0136] Serial dilutions of test compounds are prepared as described
above. Compounds are further diluted 20.times. in KH.sub.2PO.sub.4
buffer. Ten .mu.L of each dilution is added to each well on row A
to H of a corresponding low protein binding black plate containing
the reaction mixture (25 .mu.L of 50 mM KH.sub.2PO.sub.4, pH 4.6, 1
mM TRITON.RTM. X-100, 1 mg/mL Bovine Serum Albumin, and 15 .mu.M of
FRET substrate) (See Yang, et. al., J. Neurochemistry, 91(6)
1249-59 (2004)). The content is mixed well on a plate shaker for 10
minutes. Fifteen .mu.L of two hundred pM human BACE1(1-460):Fc (See
Vasser, et al., Science, 286, 735-741 (1999)) in the
KH.sub.2PO.sub.4 buffer is added to the plate containing substrate
and test compounds to initiate the reaction. The RFU of the mixture
at time 0 is recorded at excitation wavelength 355 nm and emission
wavelength 460 nm, after brief mixing on a plate shaker. The
reaction plate is covered with aluminum foil and kept in a dark
humidified oven at room temperature for 16 to 24 h. The RFU at the
end of incubation is recorded with the same excitation and emission
settings used at time 0. The difference of the RFU at time 0 and
the end of incubation is representative of the activity of BACE1
under the compound treatment. RFU differences are plotted versus
inhibitor concentration and a curve is fitted with a four-parameter
logistic equation to obtain the EC.sub.50 and IC.sub.50 values.
(See Sinha, et al., Nature, 402, 537-540 (2000)).
[0137] The following exemplified compounds were tested essentially
as described above and exhibited the following activity for
BACE1:
TABLE-US-00001 TABLE 1 Example # BACE1 IC.sub.50 (nM) 1 0.610
(.+-.0.0948, n = 8/9) 2 0.482 (.+-.0.0580, n = 6/7) 3 0.554
(.+-.0.0674, n = 3) 4 0.569 (.+-.0.0796, n = 2) 5 0.450
(.+-.0.0911, n = 4) 6 0.739 (.+-.0.181, n = 7) 7 0.358 (n = 1/3)
.sup. 8 0.730 (.+-.0.0951, n = 3) Mean .+-. SEM; SEM = standard
error of the mean
[0138] These data demonstrate that the compounds of Table 1
potently inhibit purified recombinant BACE1 enzyme activity in
vitro.
Whole Cell Assays for Measuring the Inhibition of Beta-Secretase
Activity
HEK293Swe Whole Cell Assay
[0139] The routine whole cell assay for the measurement of
inhibition of beta-secretase activity utilizes the human embryonic
kidney cell line HEK293p (ATCC Accession No. CRL-1573) stably
expressing a human APP751 cDNA containing the naturally occurring
double mutation Lys651Met652 to Asn651Leu652, commonly called the
Swedish mutation (noted HEK293Swe) and shown to overproduce Abeta
(Citron, et al., Nature, 360, 672-674 (1992)). In vitro Abeta
reduction assays have been described in the literature (See Dovey,
et al., Journal of Neurochemistry, 76, 173-181 (2001); Seubert, et
al., Nature, 361, 260 (1993); and Johnson-Wood, et al., Proc. Natl.
Acad. Sci. USA, 94, 1550-1555 (1997)).
[0140] Cells (HEK293Swe at 3.5.times.10.sup.4 cells/well,
containing 200 .mu.L culture media, DMEM containing 10% FBS) are
incubated at 37.degree. C. for 4 to 24 h in the presence/absence of
inhibitors (diluted in DMSO) at the desired concentration. At the
end of the incubation, conditioned media are analyzed for evidence
of beta-secretase activity, for example, by analysis of Abeta
peptides. Total Abeta peptides (Abeta 1-x) are measured by a
sandwich ELISA, using monoclonal 266 as a capture antibody and
biotinylated 3D6 as reporting antibody. Alternatively, Abeta 1-40
and Abeta 1-42 peptides are measured by a sandwich ELISA, using
monoclonal 2G3 as a capture antibody for Abeta 1-40, and monoclonal
21F12 as a capture antibody for Abeta 1-42. Both Abeta 1-40 and
Abeta 1-42 ELISAs use biotinylated 3D6 as the reporting antibody.
The concentration of Abeta released in the conditioned media
following the compound treatment corresponds to the activity of
BACE1 under such conditions. The 10-point inhibition curve is
plotted and fitted with the four-parameter logistic equation to
obtain the EC.sub.50 and IC.sub.50 values for the Abeta-lowering
effect. The following exemplified compounds were tested essentially
as described above and exhibited the following activity for Abeta
lowering effect:
TABLE-US-00002 TABLE 2 HEK 293 Swe A-beta HEK 293 Swe A-beta (1-40)
ELISA (1-42) ELISA Example IC.sub.50 (nM) IC.sub.50 (nM) 1 0.619
0.437 2 0.324 0.289 3 1.26 0.299 5 0.0887 0.0785 6 0.220 0.211 Mean
.+-. SEM; SEM = standard error of the mean
[0141] These data demonstrate that the compounds of Table 2
potently inhibit native Abeta production in whole cells.
PDAPP Primary Neuronal Assay
[0142] A confirmatory whole cell assay is also run in primary
neuronal cultures generated from PDAPP transgenic embryonic mice.
Primary cortical neurons are prepared from Embryonic Day 16 PDAPP
embryos and cultured in 96 well plates (15.times.10.sup.4
cells/well in DMEM/F12 (1:1) plus 10% FBS). After 2 days in vitro,
culture media is replaced with serum free DMEM/F12 (1:1) containing
B27 supplement and 2 .mu.M (final) of Ara-C (Sigma, C1768). At day
5 in vitro, neurons are incubated at 37.degree. C. for 24 h in the
presence/absence of inhibitors (diluted in DMSO) at the desired
concentration. At the end of the incubation, conditioned media are
analyzed for evidence of beta-secretase activity, for example, by
analysis of Abeta peptides. Total Abeta peptides (Abeta 1-x) are
measured by a sandwich ELISA, using monoclonal 266 as a capture
antibody and biotinylated 3D6 as reporting antibody. Alternatively,
Abeta 1-40 and Abeta 1-42 peptides are measured by a sandwich
ELISA, using monoclonal 2G3 as a capture antibody for Abeta 1-40,
and monoclonal 21F12 as a capture antibody for Abeta 1-42. Both
Abeta 1-40 and Abeta 1-42 ELISAs use biotinylated 3D6 as the
reporting antibody. The concentration of Abeta released in the
conditioned media following the compound treatment corresponds to
the activity of BACE1 under such conditions. The 10-point
inhibition curve is plotted and fitted with the four-parameter
logistic equation to obtain the EC.sub.50 and IC.sub.50 values for
the Abeta-lowering effect. The following exemplified compounds were
tested essentially as described above and exhibited the following
activity for Abeta lowering effect:
TABLE-US-00003 TABLE 3 PDAPP Neuron A-beta PDAPP Neuron A-beta
(1-40) ELISA (1-42) ELISA Example IC.sub.50 (nM) IC.sub.50 (nM) 1
0.487 (.+-.0.0946, n = 2) 0.591 (.+-.0.268, n = 2) 2 0.244 (n =
1/2) .sup. 1.22 (.+-.0.967, n = 2) 3 0.309 (.+-.0.0478, n = 2)
0.184 (.+-.0.0234, n = 2) 4 0.134 0.131 5 0.132 (.+-.0.0717, n = 2)
0.0813 6 0.279 (.+-.0.0607, n = 2) 0.308 (.+-.0.115, n = 2) 7
0.0873 0.0649 8 0.285 0.29 Mean .+-. SEM; SEM = standard error of
the mean
[0143] These data demonstrate that the compounds of Table 3
potently inhibit Abeta production in whole cells
In Vivo Inhibition of Beta-Secretase
[0144] Several animal models, including mouse, guinea pig, dog, and
monkey, may be used to screen for inhibition of beta-secretase
activity in vivo following compound treatment Animals used in this
invention can be wild type, transgenic, or gene knockout animals.
For example, the PDAPP mouse model, prepared as described in Games
et al., Nature 373, 523-527 (1995), and other non-transgenic or
gene knockout animals are useful to analyze in vivo inhibition of
Abeta and sAPPbeta production in the presence of inhibitory
compounds. Generally, 2 to 12 month old PDAPP mice, gene knockout
mice or non-transgenic animals are administered compound formulated
in vehicles, such as corn oil, cyclodextran, phosphate buffers,
PHARMASOLVE.RTM., or other suitable vehicles. One to twenty-four
hours following the administration of compound, animals are
sacrificed, and brains as well as cerebrospinal fluid and plasma
are removed for analysis of Abetas, C99, and sAPP fragments. (See
May, et al., Journal of Neuroscience, 31, 16507-16516 (2011)).
[0145] For standard in vivo pharmacology studies, animals are dosed
with various concentrations of compound and compared to a
vehicle-treated control group dosed at the same time. For some time
course studies, brain tissue, plasma, or cerebrospinal fluid is
obtained from selected animals, beginning at time 0 to establish a
baseline. Compound or appropriate vehicle is administered to other
groups and sacrificed at various times after dosing. Brain tissue,
plasma, or cerebrospinal fluid is obtained from selected animals
and analyzed for the presence of APP cleavage products, including
Abeta peptides, sAPPbeta, and other APP fragments, for example, by
specific sandwich ELISA assays. At the end of the test period,
animals are sacrificed and brain tissues, plasma, or cerebrospinal
fluid are analyzed for the presence of Abeta peptides, C99, and
sAPPbeta, as appropriate. Brain tissues of APP transgenic animals
may also be analyzed for the amount of beta-amyloid plaques
following compound treatment. "Abeta 1-x peptide" as used herein
refers to the sum of Abeta species that begin with residue 1 and
ending with a C-terminus greater than residue 28. This detects the
majority of Abeta species and is often called "total Abeta".
[0146] Animals (PDAPP or other APP transgenic or non-transgenic
mice) administered an inhibitory compound may demonstrate the
reduction of Abeta or sAPPbeta in brain tissues, plasma or
cerebrospinal fluids and decrease of beta amyloid plaques in brain
tissue, as compared with vehicle-treated controls or time zero
controls. For example, 3 hours after administration of 1, 3, or 10
mg/kg oral dose of the compound of Example 1 to young female PDAPP
mice, Abeta 1-x peptide levels are reduced approximately 34%, 48%,
and 53% in brain hippocampus, and approximately 43%, 59% and 66% in
brain cortex, respectively, compared to vehicle-treated mice.
[0147] For example, 3 hours after administration of 1 or 3 mg/kg
oral dose of the compound of Example 3, Abeta 1-x peptide levels
are reduced approximately 38% and 50% in brain hippocampus, and
approximately 34% and 53% in brain cortex, respectively compared to
vehicle-treated mice.
[0148] Given the activity of Examples 1 and 3 against BACE enzyme
in vitro, these Abeta lowering effects are consistent with BACE
inhibition in vivo, and further demonstrate CNS penetration of
Examples 1 and 3
[0149] These studies show that compounds of the present invention
inhibit BACE and are, therefore, useful in reducing Abeta
levels.
* * * * *