5-Fluoro-1,3-thiazol-2-amine → 4-(3,5-Difluoro-phenyl)-6-methyl-pyridine-2-carboxylic acid (5-fluoro-thiazol-2-yl)-amide

HRID 552548Notes

Reaction equation

HRID 552548 reaction equation
C(O[C:4]([C:6]1[CH:11]=[C:10]([C:12]2[CH:17]=[C:16]([F:18])[CH:15]=[C:14]([F:19])[CH:13]=2)[CH:9]=[C:8]([CH3:20])[N:7]=1)=[O:5])C.[F:21][C:22]1[S:26][C:25]([NH2:27])=[N:24][CH:23]=1>>[F:21][C:22]1[S:26][C:25]([NH:27][C:4]([C:6]2[CH:11]=[C:10]([C:12]3[CH:13]=[C:14]([F:19])[CH:15]=[C:16]([F:18])[CH:17]=3)[CH:9]=[C:8]([CH3:20])[N:7]=2)=[O:5])=[N:24][CH:23]=1

Participants

3

Reactant 2

HCID 100803855-Fluoro-1,3-thiazol-2-amineHCID 671639994-(3,5-Difluorophenyl)-6-methyl-pyridine-2-carboxylic acid ethyl ester

Product 1

HCID 866145954-(3,5-Difluoro-phenyl)-6-methyl-pyridine-2-carboxylic acid (5-fluoro-thiazol-2-yl)-amide

Procedure

The title compound, was prepared from 4-(3,5-Difluoro-phenyl)-6-methyl-pyridine-2-carboxylic acid ethyl ester in accordance with the general method of example 26, step 6 using 5-Fluoro-thiazol-2-ylamine (CAS: [64588-82-5], WO2006016178 instead of 3-Chloroaniline to yield the final compound as a light yellow crystalline solid, MS (ISP): m/e=350.2 (M+H)+.

Sources & evidence

ORD record
ord-d266e068f9754905b119606862949983
Source dataset
uspto-grants-2011_05
Patent number
US07951824B2

Reaction notes

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