2-Amino-4-methylthiazole → 6-Methyl-3-(pyrimidin-5-ylamino)-pyrazine-2-carboxylic acid (4-methyl-thiazol-2-yl)-amide

HRID 550592Notes

Reaction equation

HRID 550592 reaction equation
C(O[C:4]([C:6]1[C:11]([NH2:12])=[N:10][CH:9]=[C:8]([CH3:13])[N:7]=1)=[O:5])C.Br[C:15]1[CH:16]=[N:17][CH:18]=[N:19][CH:20]=1.[NH2:21][C:22]1[S:23][CH:24]=[C:25]([CH3:27])[N:26]=1>>[CH3:27][C:25]1[N:26]=[C:22]([NH:21][C:4]([C:6]2[C:11]([NH:12][C:15]3[CH:16]=[N:17][CH:18]=[N:19][CH:20]=3)=[N:10][CH:9]=[C:8]([CH3:13])[N:7]=2)=[O:5])[S:23][CH:24]=1

Participants

4

Reactant 3

HCID 741432-Amino-4-methylthiazoleHCID 783445-BromopyrimidineHCID 317738Ethyl 3-amino-6-methylpyrazine-2-carboxylate

Product 1

HCID 119964696-Methyl-3-(pyrimidin-5-ylamino)-pyrazine-2-carboxylic acid (4-methyl-thiazol-2-yl)-amide

Procedure

The title compound, MS: m/e=328.3 (M+H+), was prepared in accordance with the general method of example 10 from 3-amino-6-methyl-pyrazine-2-carboxylic acid ethyl ester (Example C), 5-bromopyrimidine and 2-amino-4-methylthiazole

Sources & evidence

ORD record
ord-25a1e54bc31f4689935abfafe3b429d5
Source dataset
uspto-grants-2011_05
Patent number
US07947685B2

Reaction notes

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