Process for water soluble azole compounds

Inactive Publication Date: 2002-05-23
EISIA R&D MANAGEMENT CO LTD
View PDF0 Cites 5 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The utility of this class of compounds is limited by their low water solubility.
This greatly impedes developing suitable parenteral dosage forms.
It was later discovered by the present inventors that use of purified reagent IlIl gave fairly low yields of intermediate IV (approximately 10-35% yield) in the above reaction, resulting in low overall yields of product I. However, when a source of iodide ion is added to the O-alkylation step of the above reaction, the yield of intermediate IV is unex

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Process for water soluble azole compounds
  • Process for water soluble azole compounds
  • Process for water soluble azole compounds

Examples

Experimental program
Comparison scheme
Effect test

example 1

Illustrates Prior Process of U.S. Ser. No. 60 / 177,169

(2R,3R)-3-[4-(4-cyanophenyl)thiazol-2-yl]-2-(2,4-difluorophenyl)-1-(1 H-1,2,4-triazol-1-yl)-2-[(dihydrogen phosphonoxy)methoxy]butane, sodium salt

[0085] 25

A. (2R, 3R)-3-[4-(4-cyanophenyl)thiazol-2-yl]-2-(2,4-difluorophenyl)-1-(1H--1,2,4-triazol-1-yl)-2-[(di-tert-butyl phosphonoxy)methoxy]butane

[0086] 26

[0087] To a solution of (2R, 3R)-3-[4-(4-cyanophenyl)thiazol-2-yl]-2-(2,4--difluorophenyl)-1-(1H-1,2,4-triazol-1-yl)butan-2-oI, II, (8.74 g, 20 mmol) in THF (40 mL) under a nitrogen atmosphere was added sodium hydride (0.80 g, 60% in oil, 20 mmol) at rt. The resulting mixture was stirred at rt for 0.25 h then di-tert-butyl chloromethyl phosphate, III (10.3 g, 40 mmol) was added. The reaction mixture was heated at 50.degree. C. for 16 h. The reaction mixture was then allowed to cool to rt and was concentrated under reduced pressure. The residue was dissolved in Et.sub.2O and was washed with H.sub.2O and brine. The organic layer was d...

example 2

(2R,3R)-3-[4-(4-cyanophenyl)thiazol-2-yl]-2-(2,4-difluorophenyl)-1-(1H-1,2-,4-triazol-1-yl)-2-[(dihydrogen phosphonoxy)methoxy]butane

[0100] 29

[0101] A. An oven dried, 1 L round-bottom flask equipped with a mechanical stirrer, nitrogen inlet adapter, pressure-equalizing addition funnel fitted with a rubber septum and temperature probe was charged with sodium hydride (2.89 g, 0.069 mol, 60%) and THF (50 mL). To this stirred suspension, (2R,3R)-3-[4-(4-cyanophenyl)thiazol-2-yl]-2-(2,4-difluorophen-yl)-1-(1H-1,2,4-triazol-1-yl)butan-2-ol, II, (10 g, 0.023 mol) in 30 mL of THF was added dropwise over 20 minutes at room temperature. After stirring for 45 minutes, a solution of iodine (2.99 g, 0.0115 mol) in THF (30 mL)) was added dropwise over 10 minutes followed by dropwise addition of di tert butylchloromethyl phosphate, III (13.29 g, 0.035 mol, .about.68% purity) over 15 minutes. The reaction mixture was stirred for 4 h at about 41.degree. C. to complete the reaction. The completion of...

example 3

Bis lysine salt of (2R,3R)-3-[4-(4-cyanophenyl)thiazol-2-yl]-2-(2,4-difluo-rophenyl)-1-(1H-1,2,4-triazol-1-yl)-2-[(dihydrogen phosphonoxy)methoxy]but-ane

[0103] The above obtained title product from Example 2 was dissolved in methanol (75 mL) and to this L-lysine (1.8 g) was added and heated at 60.degree. C. for 4.5 h. The hot reaction mixture was filtered through a bed of Celite. The filtrate was concentrated to a volume of about 5 mL, mixed with ethanol (100 mL) and heated to 65.degree. C. to crystallize the bis lysine salt. The salt was collected on a Buchner funnel and dried under vacuum to afford 3.71 g as an off white crystalline solid.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

An improved process is provided for preparing water-soluble prodrugs of triazole antifungal compounds containing a secondary or tertiary hydroxyl group. More particularly, the improved process is directed toward preparation of water-soluble triazole antifungal compounds are provided having the general formula wherein A is the non-hydroxy portion of a triazole antifungal compound of the type containing a secondary or tertiary hydroxyl group and R and R1 are as defined in the specification.

Description

[0001] This application claims the benefit of U.S. Provisional Application Serial No. 60 / 252,001 filed on Nov. 20, 2000.[0002] This invention relates to an improved process for preparing certain water-soluble azole compounds useful in the treatment of serious systemic fungal infections. More particularly, the present invention relates to an improved process for preparing the water-soluble prodrugs having the general formula 2[0003] Wherein A is the non-hydroxy portion of a triazole antifungal compound of the type containing a secondary or tertiary hydroxy group, R and R.sup.1 are each independently hydrogen or (C.sub.1-C.sub.6)alkyl, and pharmaceutically acceptable salts thereof.DESCRIPTION OF THE PRIOR ART[0004] Triazole antifungal compounds are well known in the prior art. Of the several classes known, one particularly potent class contains a tertiary hydroxyl group. For example, U.S. Pat. No. 5,648,372 discloses that (2R,3R)-3-[4-(4-cyanophenyl)thiazol-2-yl]-2-(2,4-difluorophenyl...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
IPC IPC(8): C07F9/6539C07D249/08C07D277/22C07F9/6518C07F9/6558
CPCC07F9/65583C07F9/65181C07F9/6518C07F9/09
Inventor CHEN, CHUNG-PINCONNOLLY, TIMOTHY PAULKOLLA, LAXMA REDDYMATISKELLA, JOHN D.MUELLER, RICHARD H.PENDRI, YADAGIRIPETSCH, DEJAH T.
Owner EISIA R&D MANAGEMENT CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap