U.S. patent application number 09/822945 was filed with the patent office on 2002-01-03 for process for the selective n-formylation of n-hydroxylamines.
Invention is credited to Hill, David R., Hsiao, Chi-Nung, Kurukulasuriya, Ravi, Wittenberger, Steve.
Application Number | 20020002307 09/822945 |
Document ID | / |
Family ID | 27393276 |
Filed Date | 2002-01-03 |
United States Patent
Application |
20020002307 |
Kind Code |
A1 |
Hill, David R. ; et
al. |
January 3, 2002 |
Process for the selective N-formylation of N-hydroxylamines
Abstract
The instant invention provides a process for the selective
N-formylation of N-hydroxylamines.
Inventors: |
Hill, David R.; (Gurnee,
IL) ; Hsiao, Chi-Nung; (Libertyville, IL) ;
Kurukulasuriya, Ravi; (Gurnee, IL) ; Wittenberger,
Steve; (Mundelein, IL) |
Correspondence
Address: |
Steven F. Weinstock
Abbott Laboratories
AP6D/D-377
100 Abbott Park Road
Abbott Park
IL
60064-6050
US
|
Family ID: |
27393276 |
Appl. No.: |
09/822945 |
Filed: |
March 30, 2001 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
60193973 |
Mar 31, 2000 |
|
|
|
60261640 |
Jan 12, 2001 |
|
|
|
Current U.S.
Class: |
562/621 ;
548/320.1; 549/452 |
Current CPC
Class: |
C07C 259/06 20130101;
C07D 233/74 20130101; C07D 317/28 20130101 |
Class at
Publication: |
562/621 ;
549/452; 548/320.1 |
International
Class: |
C07D 233/40; C07D
317/28; C07C 239/14 |
Claims
1. A process for the conversion of an N-hydroxylamine to an
N-hydroxyformamide comprising reacting the N-hydroxylamine with
2,2,2-trifluoroethylformate in an optionally buffered solvent.
2. A process according to claim 1, wherein the N-hydroxylamine is
selected from the group consisting of N-benzyl-N-hydroxylamine,
((1S)-1-(N-hydroxyamino)ethyl)benzene,
3-((2S)-2-(N-hydroxyamino)-3-((4'--
(trifluoromethoxy)(1,1'-biphenyl)-4-yl)oxy)propyl)-5,5'-dimethyl-2,4-dimet-
hyl-2,4-imidazolidinedione, and
(4S)-4-((1S)-1-(hydroxyamino)-2-((4-(4'-(t-
rifluoromethoxy)phenoxy)phenyl)sulfonyl)ethyl)-2,2-dimethyl-1,3-dioxolane.
3. A process according to claim 2 wherein the N-hydroxylamine is
3-((2S)-2-(N-hydroxyamino)-3-((4'-(trifluoromethoxy)(1,1'-biphenyl)-4-yl)-
oxy)propyl)-5,5'-dimethyl-2,4-dimethyl-2,4-imidazolidinedione.
4. A process according to claim 2 wherein the N-hydroxylamine is
(4S)-4-((1S)-1-(hydroxyamino)-2-((4-(4'-(trifluoromethoxy)phenoxy)phenyl)-
sulfonyl)ethyl)-2,2-dimethyl-1,3-dioxolane.
5. A process according to claim 1 wherein the buffer is selected
from the group consisting of a carbonate salt, a bicarbonate salt,
a phosphate salt, a tertiary amine, an optionally subsituted
pyridine, imidazole, and a carboxylate salt.
6. A process according to claim 5 wherein the buffer is selected
from the group consisting of imidazole and a carboxylate salt.
7. A process according to claim 6 wherien the buffer is selected
from the group consisting of imidazole and sodium formate.
8. A process according to claim 1, wherein the solvent is selected
from the group consisting of tetrahydrofuran, methyl tert-butyl
ether, ethyl acetate, isopropyl acetate, 2,2,2-trifluoroethanol,
formic acid, toluene, and mixtures thereof.
9. A process according to claim 8 wherein the solvent is selected
from the group consisting of tetrahydrofuran, isopropyl acetate,
methyl tert-butyl ether, formic acid, and mixtures thereof.
10. A process according to claim 1 which is conducted at about
50.degree. C. to about 70.degree. C.
11. A process according to claim 1 which is conducted for about 3
to about 24 hours.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application claims benefit of U.S. Provisional Patent
Applications, Serial No. 60/193,973, filed Mar. 31, 2000 and Serial
No. 60/261,640 filed Jan. 12, 2001.
TECHNICAL FIELD
[0002] This invention relates to a process for the selective
N-formylation of N-hydroxylamines.
BACKGROUND OF THE INVENTION
[0003] While there are several published methods for the
N-formylation of N-hydroxylamines, many of these routes have proven
to be problematic. Disproportionation of the hydroxylamine to
oximes and formylated primary amines is common, as is the formation
of O-formylated and N,O-bis-formylated by-products. Methods which
have proven to minimize by-product formation often require extended
reaction times and elevated temperatures, which are impractical for
large-scale preparations. Thus, there is a continuing need for an
efficient method of selectively formylating the nitrogen of an
N-hydroxylamine.
[0004] The instant invention discloses a large-scale synthesis of
N-hydroxyformamides from N-hydroxylamines and
2,2,2-trifluoroethylformate- . While the formylation of enolates
with 2,2,2-trifluoroethylformate has been disclosed (Zayia, G. H.
Organic Lett. 1999, 1, 989-991), the formylation of
N-hydroxylamines with this reagent has not previously been
described.
SUMMARY OF THE INVENTION
[0005] The process of the instant invention provides a selective
N-formylation of N-hydroxylamines to provide N-hydroxyformamides
which minimizes by-product formation.
[0006] In one embodiment of the instant invention is provided a
process for the conversion of an N-hydroxylamine to an
N-hydroxyformamide comprising reacting the N-hydroxylamine with
2,2,2-trifluoroethylformate in an optionally buffered solvent.
DETAILED DESCRIPTION OF THE INVENTION
[0007] The following terms have the meanings specified:
[0008] The term "alkyl," as used herein, represents a monovalent
group derived from a straight or branched chain saturated
hydrocarbon by the removal of a single hydrogen atom.
[0009] The term "C.sub.1-C.sub.4 alkyl group," as used herein,
represents a straight or branched chain saturated hydrocarbon
radical having from one to four carbon atoms. Alkyl groups of this
invention include methyl, ethyl, propyl, tert-butyl, and the
like.
[0010] The term "aryl," as used herein, represents phenyl,
naphthyl, dihydronaphthyl, tetrahydronaphthyl, indanyl, and
indenyl. Aryl groups having an unsaturated or partially saturated
ring fused to an aromatic ring can be attached through either the
saturated or unsaturated part of the group.
[0011] The term "arylalkyl," as used herein, represents an aryl
group attached to the parent group through an alkyl group.
[0012] The term "buffered solvent," as used herein, represents a
solvent containing an agent capable in solution of neutralizing
acids and bases and thereby maintaining a pH at or near the
original pH of a solution during the course of a reaction.
Representative buffering agents carbonate salts such as sodium
carbonate, potassium carbonate, calcium carbonate, and the like;
bicarbonate salts such as sodium bicarbonate, potassium
bicarbonate, and the like; phosphate salts such as potassium
phosphate, potassium hydrogenphosphate, sodium dihydrogenphosphate,
and the like; tertiary amines such as triethylamine,
diisopropylethylamine, and the like; optionally substituted
pyridines such as 2,6-lutidine, pyridine, collidine, and the like;
imidazole; and carboxylate salts such as sodium formate, potassium
carbonate, and the like.
[0013] The term "cycloalkyl," as used herein, represents a
monovalent saturated cyclic hydrocarbon group.
[0014] The term "(cycloalkyl)alkyl," as used herein, represents a
cycloalkyl group attached to the parent molecular moiety through an
alkylene group.
[0015] The term "--C.sub.2-C.sub.8 dialkyl ether," as used herein,
represents --R.sup.1--O--R.sup.2, wherein R.sup.1 and R.sup.2 are
independently a C.sub.1-C.sub.4 alkyl group, or, R.sup.1 and
R.sup.2, together with the oxygen atom to which they are attached,
form a tetrahydrofuranyl or tetrahydropyranyl ring.
[0016] The term "electron-withdrawing group," as used herein,
represents a group which draws electrons to itself more than a
hydrogen atom occupying the same position in the molecule would.
Examples of electron-withdrawing groups include alkanoyl,
arylsulfonyl, alkylsulfonyl, and the like.
[0017] The term "heteroaryl," as used herein, represents a cyclic
aromatic group having five or six ring atoms wherein at least one
ring atom is selected from the group consisting of oxygen, sulfur,
and nitrogen, and the remaining ring atoms are carbon. Heteroaryl
groups of this invention include those derived from furan,
imidazole, isoquinoline, isothiazole, isoxazole, oxadiazole,
oxazole, 1,2,3-oxadiazole, pyrazine, pyrazole, pyridazine,
pyridine, pyrimidine, pyrroline, quinoline, thiazole,
1,3,4-thiadiazole, thiene, triazole, and tetrazole.
[0018] The term "heteroarylalkyl," as used herein, represents a
heteroaryl group attached to the parent molecular moiety through an
alkyl group.
[0019] The term "N-hydroxylamine," as used herein, represents
NHR.sup.3(OR.sup.4), wherein R.sup.3 is any group considered by
those skilled in the art to be stable under the reaction
conditions; and R.sup.4 is selected from the group consisting of
hydrogen, alkyl, aryl, arylalkyl, cycloalkyl, (cycloalkyl)alkyl,
heteroaryl, and heteroarylalkyl.
[0020] The term "N-hydroxyformamide," as used herein, represents
NR.sup.3(CHO)(OR.sup.4), wherein R.sup.3 and R.sup.4 have been
previously defined.
[0021] The term "substituted pyridine," as used herein, represents
a pyridine optionally substituted with one, two, or three methyl
groups. Examples of substituted pyridines include 2-picoline;
3-picoline; 4-picoline; 2,6-lutidine; 2,5-lutidine; 2,4-lutidine;
2,4,6-collidine; 2,3,5-collidine; and the like.
[0022] Synthetic Processes
[0023] The compounds and process of the instant invention will be
better understood in connection with the following synthetic scheme
which illustrates the method by which the compounds of the instant
invention are prepared. 1
[0024] As shown in Scheme 1, compounds of formula (1) can be
converted to compounds of formula (3) by treatment with
2,2,2-trifluoroethyl formate (2), which can be prepared according
to the procedure described in J. Chem. Soc. B 1971, 826-831.
Examples of solvents used in these reactions include
tetrahydrofuran, methyl tert-butyl ether, diethyl ether, ethyl
acetate, isopropyl acetate, 2,2,2-trifluorethanol, formic acid,
toluene, and mixtures thereof. The reaction temperature is about
35.degree. C. to about 75.degree. C. and depends on the solvent
chosen. Reaction times are typically about 4 to about 18 hours.
When the compounds of formula (1) or the compounds of formula (3)
are acid-sensitive, the reaction is preferably buffered.
Representative buffering agents include carbonate salts,
bicarbonate salts, phosphate salts, tertiary amines, optionally
substituted pyridines, imidazole, and carboxylate salts.
Preferably, the buffer is either imidazole or a carboxylate salt.
More preferably, the buffer is either imidazole or sodium
formate.
EXAMPLE 1
(1S)-2-(4,4-dimethyl-2,5-dioxo-1-imidazolidinyl)-1-(((4'-(trifluoromethoxy-
)(1,1'-biphenyl)-4-yl)oxy)methyl)ethyl-(N-hydroxy)formamide
[0025] A solution of
3-((2S)-2-(N-hydroxyamino)-3-((4'-(trifluoromethoxy)(-
1,1'-biphenyl)-4-yl)oxy)propyl)-5,5-dimethyl-2,4-imidazolidinedione,
para toluene sulfonic acid salt (1.95 kg, prepared according to the
procedure described in commonly owned WO 99/06361) in 15% (w/w)
potassium carbonate (4.29 kg), tetrahydrofuran (5.07 kg), and
methyl tert-butyl ether (4.12 kg) was stirred until all solids
dissolved and separated into an aqueous fraction and an organic
fraction. The organic fraction was washed with 25% (w/w) sodium
chloride (3.83 kg), treated with tetrahydrofuran (0.58 kg), and
concentrated to provide a 20-30% (w/w) solution of the free base.
The solution was treated with the 2,2,2-trifluoroethyl formate
reagent (5.27 kg of the 71.9% (w/w) solution (3.79 kg, 10
equivalents), stirred at reflux for 4 hours, cooled to less than
30.degree. C., treated with water (5.33 kg) and methyl tert-butyl
ether (7.62 kg), washed with 15% (w/w) potassium bicarbonate (5.3
kg portions) until the pH of the wash was .gtoreq.8, and
concentrated. The residue was dissolved in ethyl acetate (7.133
kg), treated with heptane (10.71 kg) during which a solid began to
precipitate, stirred for 18 hours, and filtered. The filter cake
was rinsed with 1:2 (v/v) ethyl acetate/heptane (5.63 kg), suction
dried, then vacuum dried (100 mm Hg) at 100.degree. C. with a
nitrogen bleed to provide 2.685 kg (91.8%, >99% ee) of the
desired product. .sup.1H NMR (300 MHz, DMSO-d.sub.6) .delta.9.95
(br s, 0.5H), 9.80 (br s, 0.5H), 8.41 (br s, 0.5H), 8.37 (br s,
0.5H), 8.35 (s, 0.5H), 7.95 (s, 0.5H), 7.76 (d, 2H, J=8.9 Hz), 7.65
(d, 2H, J=8.5 Hz), 7.43 (d, 2H, J=8.5 Hz), 7.04 (d, 2H, J=8.9 Hz),
4.92-4.80 (m, 0.5H), 4.50-4.38 (m, 0.5H), 4.28-4.06 (m, 2H),
3.82-3.68 (m, 1H), 3.66-3.54 (m, 1H), 3.88 (s, 3H), 3.84 (s,
3H).
EXAMPLE 2
N-hydroxy((1S)-1-phenylethyl)formamide
EXAMPLE 2A
(1S)-N-((4-methoxyphenyl)methylidene)-1-phenylethanamine
[0026] A mixture of p-anisaldehyde (11.24 g, 82.5 mmol) and
(S)-.alpha. methyl benzyl amine (10.0 g, 82.5 mmol) in toluene (100
mL) was heated to reflux with removal of water by a Dean-Stark
apparatus. After cooling to ambient temperature, the mixture was
concentrated to provide 20.15 g (100%) of the desired product.
.sup.1H NMR (300 MHz, CDCl.sub.3) .delta.8.30 (s, 1H), 7.75-7.68
(m, 2H), 7.45-7.15 (m, 5H), 4.50 (q, 1H, J=6.6 Hz), 3.82 (s, 3H),
1.58 (d, 3H, J=6.6 Hz).
EXAMPLE 2B
N-((1S)-1-phenylethyl)hydroxylamine
[0027] A -78.degree. C. solution of Example 2A (7.15 g, 30 mmole)
in tetrahydrofuran (75 mL) was treated with a solution of
3-chloroperoxybenzoic acid (15 g, 60 mmol), warmed to 0.degree. C.,
stirred for 2 hours, diluted with ethyl acetate (100 mL), washed
sequentially with 10% (w/w) sodium thiosulfate, saturated sodium
bicarbonate, and brine, dried (MgSO.sub.4), filtered, and
concentrated. The concentrate was dissolved in tetrahydrofuran (100
mL), treated with p-toluene sulfonic acid monohydrate (8.15 g, 42.8
mmol), stirred for 2 hours, treated with a solution of
N-hydroxylamine hydrochloride (8.7 g) in water (15 mL), and stirred
for 16 hours. The mixture was diluted with ethyl acetate (100 mL),
washed with saturated sodium bicarbonate and brine, dried
(MgSO.sub.4), filtered, and concentrated. The concentrate was
purified by flash column chromatography on silica gel with 1:2
ethyl acetate/hexanes to provide 3.53 g (86% yield) of the desired
product. .sup.1H NMR (300 MHz, CDCl.sub.3) .delta.7.36-7.20 (m,
5H), 4.09 (q, 1H, J=6.6 Hz), 1.48 (d, 3H, J=6.6 Hz).
EXAMPLE 2C
N-hydroxy((1S)-1-phenylethyl)formamide
[0028] A solution of Example 2B (1.5 g, 10.95 mmol) in
tetrahydrofuran (15mL, 10 vols) was treated with the
2,2,2-trifluoroethyl formate reagent (92% wt, 7.6 g, 54.7 mmol, 5
equiv). The resulting mixture was heated at 65.degree. C. for 18
hours and concentrated. The concentrate was distilled under vacuum
(170.degree. C. at 1.6 mm Hg) to provide 1.6 g (89%) of the desired
product. .sup.1H NMR (300 MHz, CDCl.sub.3) .delta.8.00 (s, 1H),
7.54-7.30 (m, 5H), 4.93 (q, 1H, J=7 Hz), 1.82 (d, 3H, J=7 Hz).
EXAMPLE 3
benzyl-(N-hydroxy)formamide
[0029] A suspension of N-benzyl-N-hydroxylamine hydrochloride (1.0
g, 6.26 mmol; Aldrich Chemical Company, Milwaukee, Wis.) in methyl
tert-butyl ether (10 mL) was vigorously stirred 10% potassium
bicarbonate solution and separated into an aqueous fraction and an
organic fraction. The organic fraction was treated with the
2,2,2-trifluoroethyl formate reagent (92% (w/w), 4.35 g, 31.3 mmol,
5 equiv), and heated at reflux for 6 hours. The mixture was washed
sequentially with water, 15% potassium bicarbonate, and 15% brine,
then concentrated to provide 0.90 g (96%) of the desired product as
a mixture of rotamers. .sup.1H NMR (300 MHz, CDCl.sub.3)
.delta.8.28, 7.86 (2s, 1H total), 7.35-7.15 (m, 5H total), 7.10,
6.90 (2 br s, 1H total), 4.64, 4.56 (2s, 2H total).
EXAMPLE 4
(1S)-1-((4S)-2,2-dimethyl-1,3-dioxolan-4-yl)-2-((4-(4'-(trifluoromethoxy)p-
henoxy)phenyl)sulfonyl)ethyl(hydroxy)formamide
EXAMPLE 4A
1-(methylsulfonyl)-4-(4'-(trifluoromethoxy)phenoxy)benzene
[0030] A solution of 1-fluoro-4-(methylsulfonyl)benzene (2.2 kg),
KOH (906.3 g), 4-(trifluoromethoxy)phenol (2.364 kg) and DMSO (4.4
L) was heated to 90.degree. C. and stirred until HPLC showed
<0.5% starting material remained (about 10 hours). HPLC
conditions: Zorbax SB-C8 4.6 mm.times.25 cm; mobile phase was a
gradient of 70% water with 0.1% H.sub.3PO.sub.4/30% acetonitrile to
10% water with 0.1% H.sub.3PO.sub.4/90% acetonitrile over 15
minutes at a flow rate of 1.5 mL/min, followed by a five minute
hold at 10/90; UV detection at 220 nM. Retention times: starting
sulfone, 4.5 min; desired product, 7.8 min.
[0031] The reaction mixture was cooled to room temperature, diluted
with water (8.8 kg), and extracted with two portions of toluene (24
L and 4.7 L). The combined extracts were washed with 1N NaOH
solution (11 kg) and water (2.times.11 kg), filtered, concentrated
to a volume of approximately 6 L, treated with heptane (22 L) with
agitation, stirred for 2 hours, and cooled to 0-5.degree. C. until
the mother liquor was assayed for the desired product at <5
mg/mL. The precipitate was filtered, washed with heptane (6.6 L)
and dried under vacuum (100 mm Hg with nitrogen sweep) at
40.degree. C. to provide 2.0 kg (96.4% wt potency, 89.6% yield) of
the desired product. Recrystallization from methanol/water (4:8
v/v) gave the purified product with 98% recovery.
[0032] .sup.1H NMR (300 MHz, CDCl.sub.3) .delta.7.9 (d, 2H), 7.3
(br d, 2H), 7.1 (d, 4H), 3.1 (s, 3H).
EXAMPLE 4B
1-((4R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2-((4-(4'-(trifluoromethoxy)phenox-
y)phenyl)sulfonyl)ethanone
[0033] A solution of Example 4A (3.327 kg, 98.7% potency, 9.88 mol)
in THF (23 L, pre-dried with 3A molecular sieves) in a flask
equipped with an overhead stirrer, an addition funnel, a
temperature probe, and a nitrogen inlet was cooled to
<-40.degree. C. and treated with 1M LiHMDS in THF (10.08 L,
10.08 mmol) at such a rate as to keep the internal temperature
<-40.degree. C. The solution was treated with 2.28M
n-butyllithium in hexanes (2.275 L, 5.187 mol), treated with 2.42M
n-butyllithium (2.143 L, 5.187 mol) at such a rate as to keep the
internal temperature <-40.degree. C., and stirred for 2 hours.
The solution was treated with a solution of
(R)-methyl-O-isopropylidene glycerate (1.77 kg, 11.066 mol, 1.12
equivalents) in THF (1.77 kg) at such a rate as to keep the
internal temperature <-40.degree. C. The resulting mixture was
stirred until <1% starting material was observed by HPLC (about
1 hour). HPLC conditions: Zorbax SB-C8 4.6mm.times.25 cm column;
mobile phase was a gradient of 70% water with 0.1%
H.sub.3PO.sub.4/30% acetonitrile to 10% water with 0.1%
H.sub.3PO.sub.4/90% acetonitrile over 15 minutes at a flow rate of
1.5 mL/min; followed by 5 minute hold at 10/90; UV detection at 210
nM. Retention times: starting material, 7.8 min; desired product,
15.2 min.
[0034] The mixture was warmed to -25.degree. C. and the reaction
was adjusted to pH 5.5 with 2N H.sub.2SO.sub.4 (a pH range between
4-6 was optimal to avoid cleavage of the acetonide group and
racemization). The internal temperature of the reaction mixture was
allowed to rise to between 0.degree. C. and 5.degree. C. during the
acid addition giving a clear biphasic solution and allowing
accurate measurement of the pH via a pH meter. The solution was
treated with isopropyl acetate (33.27 L), stirred, and allowed to
settle. The organic phase was washed sequentially with water (14.48
L), 5% NaHCO.sub.3 solution (14.65 kg), and 15% NaCl solution
(14.50 kg), and azeotropically distilled with THF until <10%
isopropyl acetate remained as determined by gas chromatography.
GC-FID conditions: Stabilwax-DB column (Restek Corp. cat#10823,
lot#15531A, L=30m, ID=0.25 mm), heater at 250.degree. C., oven
temperature gradient: 40.degree. C. for 0 to 4 min then 10.degree.
C./min to 100.degree. C., then hold at 100.degree. C. 10 min,
post-run 5 min; 1 .mu.L injection volume. Peak identification: THF,
4.12 min; isopropyl acetate, 4.34 min.
[0035] The solution was filtered and concentrated to a weight of
approximately 8 kg to provide a solution of the desired product
which was used without further purification. However, the final
product could be purified by crystallization from isopropyl acetate
to provide a white crystalline solid.
[0036] .sup.1H NMR (300 MHz, CDCl.sub.3) .delta.7.93-7.85 (m, 2H),
7.33-7.25 (m, 2H), 7.20-7.05 (m, 4H), 4.62 (d, 1H), 4.58-4.52 (dd,
1H), 4.30 (d, 1H), 4.22-4.09 (m, 2H), 1.46 (s, 3H), 1.38 (s,
3H).
EXAMPLE 4C
1-((4R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2-((4-(4'-(trifluoromethoxy)phenox-
y)phenyl)sulfonyl)ethanol
[0037] A mixture of NaBH.sub.4 (240 g) and ethanol (9.8 L) at
-5.degree. C. was treated with Example 4B (either isolated or as a
THF solution) (4.53 kg, 10.53 mol by assay) and stirred until HPLC
showed none of the starting ketone remaining. HPLC conditions:
Zorbax SB-C8 4.6 mm.times.25 cm, mobile phase was a gradient of 70%
water with 0.1% H.sub.3PO.sub.4/30% acetonitrile to 10% water with
0.1% H.sub.3PO.sub.4/90% acetonitrile over 15 minutes at a flow
rate of 1.5 mL/min; followed by 5 minute hold at 10/90; UV
detection at 220 nM. Retention times: starting material, 15 min;
desired products (2 diastereomers), 7.8 and 7.9 min.
[0038] The mixture was quenched with 2N acetic acid at such a rate
as to keep the internal temperature <30.degree. C., concentrated
under vacuum at <40.degree. C. to a volume of approximately 9.8
L, and dissolved in ethyl acetate (49 L). The mixture was washed
with water (24.5 L) and 15% wt NaCl solution (24.5 L), concentrated
to a volume of approximately 9.8 L, azeotropically distilled with
ethyl acetate (49 L) to a final volume of approximately 9.8 L, and
dissolved in ethyl acetate (44 L) to provide a solution of the
desired product which was used directly in the next step.
[0039] .sup.1H NMR (300 MHz, CDCl.sub.3) .delta.7.9 (d, 2H), 7.3
(br d, 2H), 7.1 (m, 4H), 4.1-3.9 (m, 4H), 3.55 (dd, 1H), 3.4-3.1
(m, 3H), 1.43, 1.35, 1.30, 1.23 (s, s, s, s, total of 6H from 2
diastereomers).
EXAMPLE 4D
(4S)-2,2-dimethyl-4-((E)-2-((4-(4'-(trifluoromethoxy)phenoxy)phenyl)sulfon-
yl)ethenyl)-1,3-dioxolane
[0040] A solution of Example 4C in ethyl acetate (5.00 kg, 10.53
mol theoretical) and triethylamine (4.32 kg) was cooled to
-5.degree. C., treated with methanesulfonyl chloride (1.94 kg) at
such a rate as to maintain the internal reaction temperature at
<10.degree. C., stirred at 0-5.degree. C. for 1 hour, and then
warmed to room temperature until HPLC showed no more than 0.5%
starting material or mesylate intermediate (about 4-8 hours). HPLC
conditions: Zorbax SB-C8 4.6 mm.times.25 cm, mobile phase was a
gradient of 70% water with 0.1% H.sub.3PO.sub.4/30% acetonitrile to
10% water with 0.1% H.sub.3PO.sub.4/90% acetonitrile over 15
minutes at a flow rate of 1.5 mL/min; followed by 5 minute hold at
10/90; UV detection at 220 nM. Retention times: starting material,
7.8 and 7.9 min; mesylate intermediate, 15.5 min; product, trans
vinyl sulfone, 16.0 min; cis vinyl sulfone, 17.1 min. Typical
trans/cis ratio is 10:1.
[0041] The reaction was quenched with water (14.6 kg) and the
organic layer was washed with 10% wt citric acid solution (19.6
kg), followed successively by 10% wt NaHCO.sub.3 solution (19.6 kg)
and water (19.6 kg). The organic layer was concentrated to a volume
of approximately 9.8 L, azeotropically distilled with MTBE
(2.times.49L), and concentrated to a final volume of approximately
9.8 L. The residue was dissolved in MTBE (49 L), and assayed for
residual ethyl acetate by gas chromatography. If ethyl acetate was
<5% in area, additional MTBE (25 L) was added to provide the
desired product as a solution. If ethyl acetate was >5% in area,
an additional azeotropic distillation with MTBE was performed.
[0042] .sup.1H NMR (300 MHz, CDCl.sub.3) .delta.7.1 (m, 4H), 6.9
(dd, 1H), 6.65 (dd, 1H), 4.7 (m, 1H), 4.2 (dd, 1H), 3.7 (dd, 1H),
1.43 (s, 3H), 1.4 (s, 3H).
EXAMPLE 4E
(4S)-4-((1S)-1-(hydroxyamino)-2-((4-(4'-(trifluoromethoxy)phenoxy)phenyl)s-
ulfonyl)ethyl)-2,2-dimethyl-1,3-dioxolane
[0043] A solution of Example 4D in MTBE was cooled to -15.degree.
C., treated with 50% wt aqueous NH.sub.2OH over a period of 30
minutes at such a rate as to keep the internal temperature between
-10.degree. C. and -15.degree. C., and stirred until HPLC showed
<0.5% starting material (about 7 to 20 hours). HPLC conditions:
Zorbax SB-C8 4.6 mm.times.25 cm, mobile phase was a gradient of 70%
water with 0.1 % H.sub.3PO.sub.4/30% acetonitrile to 10% water with
0.1% H.sub.3PO.sub.4/90% acetonitrile over 15 minutes at a flow
rate of 1.5 mL/min; followed by 5 minute hold at 10/90; UV
detection at 220 nM. Retention times: trans vinyl sulfone, 16.0
min; cis vinyl sulfone, 17.1 min; product (syn), 7.6 min; product
(anti), 8.0 min.
[0044] The mixture was warmed to room temperature, and the organic
layer was concentrated to a volume of approximately 9.8 L while
maintaining a temperature of <30.degree. C. The residue was
dissolved in ethyl acetate (74 L), washed with 15% wt NaCl solution
(2.times.19.6 L) and concentrated to a volume of approximately 9.8
L. The mixture was azeotropically distilled with MTBE (2.times.49
L) to a final volume of 9.8 L with <10% ethyl acetate relative
to MTBE. The concentration of product in solution was adjusted to
40-45% by weight by the removal or addition of MTBE, heptane (14.7
L) was slowly added, and the resulting slurry was stirred for at
least 4 hours until the concentration of product in the mother
liquor was <30 mg/mL. The precipitate was filtered, washed with
cold MTBE/heptane (1:3 v/v, 9.8 L), and dried under vacuum (100
mmHg with nitrogen sweep) at 30.degree. C. to provide 4.82 kg
(63.6%) of the desired product with 0.74% of the anti
diastereomer.
[0045] .sup.1H NMR (300 MHz, CDCl.sub.3) .delta.7.9 (d, 2H), 7.3
(d, 2H), 7.1 (br d, 4H), 4.35 (m, 1H), 4.05 (dd, 1H), 3.8 (dd, 1H),
3.6 (m, 1H), 3.45 (m, 1H), 3.1 (dd, 1H), 1.4 (s, 3H), 1.35 (s,
3H).
EXAMPLE 4F
(1S)-1-((4S)-2,2-dimethyl-1,3-dioxolan-4-yl)-2-((4-(4'-(trifluoromethoxy)p-
henoxy)phenyl)sulfonyl)ethyl(hydroxy)formamide
[0046] A 100 L flask equipped with an overhead stirrer, a nitrogen
inlet, a reflux condenser, and a thermocouple was charged with
Example 4E (3.5 kg), sodium formate (0.350 kg), isopropyl acetate
(30.45 kg), 2,2,2-trifluoroethyl formate (9.50 kg), and formic acid
(1.05 kg). The mixture was heated to an internal temperature
60.degree. C. and maintained at this temperature with continuous
stirring until HPLC showed less than 0.5% starting material (about
5 hours). HPLC conditions: Luna C-8 Phenomenex column at 20.degree.
C., mobile phase was a gradient of 55% KH.sub.2PO.sub.4 buffer (pH
2.3)/45% acetonitrile to 33/67 over 55 min at a flow rate of 1
mL/min; UV detection at 210 nM. Retention times: starting material,
41.4, product, 32.3 min.
[0047] The reaction was cooled to <30.degree. C. and treated
with 5% wt sodium chloride solution (17.68 kg). The organic phase
was washed with 5% wt sodium bicarbonate solution (17.79 kg
portions) until the pH of aqueous layer was >8.0, washed with 5%
wt sodium chloride solution (17.68 kg) (aqueous phase pH 7.0),
stored at ambient temperature for two days, and then combined with
product obtained from a second formylation reaction (3.27 kg) to
provide approximately 6.60 kg of combined product. The solutions
were combined and distilled under vacuum. Residual
2,2,2-trifluoroethanol was removed by azeotropic distillation with
isopropyl acetate and monitored by gas chromatography until the
ratio of isopropyl acetate to 2,2,2-trifluoroethanol was 1000:1.
GC-FID conditions: Stabilwax-DB column (Restek Corp. cat#10823,
lot#15531A, L=30m, ID=0.25mm), heater at 250.degree. C., oven
temperature gradient: 40.degree. C. from 0 to 4 min then 10.degree.
C./min to 100.degree. C., then held at 100.degree. C. 10 min,
post-run 5 min; 1 .mu.L injection volume. Retention times:
isopropyl acetate, 4.5 min, 2,2,2-trifluoroethanol, 9.5 min.
[0048] The concentration of the solution was adjusted by solvent
removal under vacuum to 25% wt product in isopropyl acetate. The
solution was treated with heptanes (20 L) and stirred for 15 hours,
at which time the concentration of product in the mother liquor was
measured by HPLC at 11 mg/mL. The product was collected by
filtration, rinsed with a solution of 1:1 (v/v) isopropyl
acetate/heptanes (10 L), and dried under vacuum (100 mm Hg with a
nitrogen sweep at 55.degree. C.) to provide 5.89 kg (89% yield) of
the desired product with a chiral purity of 99.8% ee. Chiral HPLC
conditions: Daicel Chiral PAK AD 4.6.times.250 mm column at ambient
temperature 0.3% v/v trifluoroacetic acid in ethanol (200 proof)
over 30 minutes with a flow rate of 0.3 mL/min, UV detection at 243
nM. Retention times: desired product, .about.17 min; enantiomer,
.about.14 min.
[0049] .sup.1H NMR (300 MHz, CDCl.sub.3) .delta.8.40 (s, 1H),
7.85-7.90 (m, 0.5H), 7.80-7.90 (m, 2H), 7.20-7.35 (m, 2H),
7.05-7.15 (m, 4H), 4.75-4.85 (m, 0.5H), 4.20-4.35 (m, 2H), 4.0-4.15
(m, 1H), 3.75-3.90 (m, 2H), 3.35 (dd, 0.5 H), 3.10 (dd, 0.5H), 1.42
(s, 3H), 1.30 (s, 3H); two rotomers of the formamide are observed
for some signals.
What is claimed is
* * * * *