3-Bromo-5-fluoropyridine → 3-(5-Fluoro-pyridin-3-ylamino)-6-methyl-pyridine-2-carboxylic acid (4-cyclopropyl-thiazol-2-yl)-amide

HRID 2219544Notes

Reaction equation

HRID 2219544 reaction equation
[CH:1]1([C:4]2[N:5]=[C:6]([NH:9][C:10]([C:12]3[C:17]([NH2:18])=[CH:16][CH:15]=[C:14]([CH3:19])[N:13]=3)=[O:11])[S:7][CH:8]=2)[CH2:3][CH2:2]1.Br[C:21]1[CH:22]=[N:23][CH:24]=[C:25]([F:27])[CH:26]=1>>[CH:1]1([C:4]2[N:5]=[C:6]([NH:9][C:10]([C:12]3[C:17]([NH:18][C:21]4[CH:22]=[N:23][CH:24]=[C:25]([F:27])[CH:26]=4)=[CH:16][CH:15]=[C:14]([CH3:19])[N:13]=3)=[O:11])[S:7][CH:8]=2)[CH2:2][CH2:3]1

Participants

3

Reactant 2

HCID 8202063-Bromo-5-fluoropyridineHCID 866075893-Amino-6-methyl-pyridine-2-carboxylic acid (4-cyclopropyl-thiazol-2-yl)-amide

Product 1

HCID 116750763-(5-Fluoro-pyridin-3-ylamino)-6-methyl-pyridine-2-carboxylic acid (4-cyclopropyl-thiazol-2-yl)-amide

Procedure

The title compound, was prepared from 3-Amino-6-methyl-pyridine-2-carboxylic acid (4-cyclopropyl-thiazol-2-yl)-amide in accordance with the general method of example 20 using 3-Bromo-5-fluoropyridine instead of 3-bromopyridine to yield the final compound as a yellow solid, MS (ISP): m/e=370.1 (M+H+).

Sources & evidence

ORD record
ord-8cb3f2eec39a4a8d8d85d339d3832306
Source dataset
uspto-grants-2008_08
Patent number
US07414060B2

Reaction notes

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