1-methyl-1H-imidazole-5-carboxylic acid → HCID 11417849, compound
Reaction equation
[O:1]1[CH2:7][CH:6]([C:8]2[C:16]3[S:15][C:14]([NH2:17])=[N:13][C:12]=3[C:11]([O:18][CH3:19])=[CH:10][CH:9]=2)[CH2:5][O:4][CH2:3][CH2:2]1.[CH3:20][N:21]1[C:25]([C:26](O)=[O:27])=[CH:24][N:23]=[CH:22]1>>[O:4]1[CH2:5][CH:6]([C:8]2[C:16]3[S:15][C:14]([NH:17][C:26]([C:25]4[N:21]([CH3:20])[CH:22]=[N:23][CH:24]=4)=[O:27])=[N:13][C:12]=3[C:11]([O:18][CH3:19])=[CH:10][CH:9]=2)[CH2:7][O:1][CH2:2][CH2:3]1Participants
3
Procedure
Using 7-[1,4]dioxepan-6-yl-4-methoxy-benzothiazol-2-ylamine and 3-methyl-3H-imidazole-4-carboxylic acid, the title compound was prepared. MS: m/e=389(M+H+).
Sources & evidence
- ORD record
- ord-0d3609ab833046299baa9e7d25f85456
- Source dataset
- uspto-grants-2008_05
- Patent number
- US07371748B2
Reaction notes
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