Isonicotinic Acid → HCID 11463282, 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.[C:20](O)(=[O:27])[C:21]1[CH:26]=[CH:25][N:24]=[CH:23][CH:22]=1>>[O:4]1[CH2:5][CH:6]([C:8]2[C:16]3[S:15][C:14]([NH:17][C:20](=[O:27])[C:21]4[CH:26]=[CH:25][N:24]=[CH:23][CH:22]=4)=[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 isonicotinic acid, the title compound was prepared. MS: m/e=386(M+H+).
Sources & evidence
- ORD record
- ord-2dd361ec304d446d9a8bd60ab36f77b1
- Source dataset
- uspto-grants-2008_05
- Patent number
- US07371748B2
Reaction notes
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