2-Amino-4-methylthiazole → HCID 11996466, compound
Reaction equation
CO[C:3]([C:5]1[C:10]([NH:11][C:12]2[CH:13]=[N:14][CH:15]=[N:16][CH:17]=2)=[N:9][CH:8]=[CH:7][N:6]=1)=[O:4].[NH2:18][C:19]1[S:20][CH:21]=[C:22]([CH3:24])[N:23]=1>>[CH3:24][C:22]1[N:23]=[C:19]([NH:18][C:3]([C:5]2[C:10]([NH:11][C:12]3[CH:13]=[N:14][CH:15]=[N:16][CH:17]=3)=[N:9][CH:8]=[CH:7][N:6]=2)=[O:4])[S:20][CH:21]=1Participants
3
Procedure
The title compound, MS: m/e=314.0 (M+H+), was prepared in accordance with the general method of example 1, step 2 from 3-(pyrimidin-5-ylamino)-pyrazine-2-carboxylic acid methyl ester and 2-amino-4-methylthiazole.
Sources & evidence
- ORD record
- ord-f7015640cba74aca8b4dd037f5a51763
- Source dataset
- uspto-grants-2011_05
- Patent number
- US07947685B2
Reaction notes
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