IP Library Granted Patent US 8,263,769
Granted Patent B2
US 8,263,769 · App. 12/669,002 · Granted Sep 11, 2012

Process for preparing voriconazole

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Quick Facts
Patent No.
US 8,263,769
App. No.
12/669,002
Granted
Sep 11, 2012
Kind
B2
Abstract

Optically pure voriconazole can be prepared in a high yield by a) subjecting 1-(2,4-difluorophenyl)-2(1H-1,2,4-triazol-1-yl)ethanone to Reformatsky-type coupling reaction with a substituted thiopyrimidine derivative to obtain a desired (2R,3S)/(2S,3R)-enantiomeric pair; b) removing the thiol derivative from the enantiomer to obtain racemic voriconazole; and c) isolating the racemic voriconazole by way of optical resolution using an optically active acid.

Claims (16)

1. A process for preparing voriconazole of formula (I), which comprises the steps of:

a) subjecting the compound of formula (IV) to Reformatsky-type coupling reaction with a compound of formula (V) to obtain a compound of formula (III) which is a (2R,3S)/(2S,3R)-enantiomeric pair;

b) removing the thiol derivative from the compound of formula (III) to obtain the racemic voriconazole of formula (II); and

c) isolating the compound of formula (II) by way of optical resolution using an optically active acid:

wherein,

R is C 1 -C 4 alkyl, benzothiazolyl, benzoxazolyl, imidazolyl, 1-methylimidazolyl, thiazolyl, pyridyl, pyrimidyl, phenyl, or phenyl having one or two substituents selected from the group consisting of halogen, nitro and methoxy.

2. The process of claim 1 , wherein step b) is carried out by using zinc and ammonium formate.

3. The process of claim 2 , wherein the zinc is used in an amount ranging from 3 to 10 equivalents based on the compound of formula (III).

4. A compound of formula (V):

wherein,

R is C 1 -C 4 alkyl, benzothiazolyl, benzoxazolyl, imidazolyl, 1-methylimidazolyl, thiazolyl, pyridyl, pyrimidyl, phenyl, or phenyl having one or two substituents selected from the group consisting of halogen, nitro and methoxy.

5. The compound of claim 4 , which is (i) 4-(1-bromo-ethyl)-6-(4-phenylsulfanyl)-5-fluoropyrimidine or (ii) 4-(1-bromo-ethyl)-6-(4-chloro-phenylsulfanyl)-5-fluoropyrimidine.

6. An enantiomeric compound of formula (III):

wherein,

R is C 1 -C 4 alkyl, benzothiazolyl, benzoxazolyl, imidazolyl, 1-methylimidazolyl, thiazolyl, pyridyl, pyrimidyl, phenyl, or phenyl having one or two substituents selected from the group consisting of halogen, nitro and methoxy.

7. The compound of claim 6 , which is (i) (2R,3S)/(2S,3R)-3-[6-(4-phenylsulfanyl)-5-fluoro-pyrimidine-4-yl]-2-(2,4-difluoro-phenyl)-1-[1,2,4]triazol-1-yl-butane-2-ol or (ii) (2R,3S)/(2S,3R)-3-[6-(4-chloro-phenylsulfanyl)-5-fluoro-pyrimidine-4-yl]-2-(2,4-difluoro-phenyl)-1-[1,2,4]triazol-1-yl-butane-2-ol.

Assignments (3)
CHANGE OF NAME Recorded Aug 3, 2012
From: HANMI HOLDINGS CO., LTD.
To: HANMI SCIENCE CO., LTD.
Reel/Frame 028722/0332 →
CHANGE OF NAME Recorded Jan 7, 2011
From: HANMI PHARM. CO., LTD.
To: HANMI HOLDINGS CO., LTD.
Reel/Frame 025599/0842 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 15, 2010
From: MOON, YOUNG HO; LEE, MOON SUB; YOO, JAE HO; KIM, JI SOOK; KIM, HAN KYONG; CHOI, CHANG JU; CHANG, YOUNG KIL; LEE, GWAN SUN
To: HANMI PHARM. CO., LTD.
Reel/Frame 023793/0180 →