2-Amino-4-methylbenzothiazole → HCID 8840491, compound
Reaction equation
[CH3:1][C:2]1[C:7]2[N:8]=[C:9]([NH2:11])[S:10][C:6]=2[CH:5]=[CH:4][CH:3]=1.[Cl:12][C:13]1[N:21]=[CH:20][CH:19]=[CH:18][C:14]=1[C:15](Cl)=[O:16]>>[Cl:12][C:13]1[N:21]=[CH:20][CH:19]=[CH:18][C:14]=1[C:15]([NH:11][C:9]1[S:10][C:6]2[CH:5]=[CH:4][CH:3]=[C:2]([CH3:1])[C:7]=2[N:8]=1)=[O:16]Participants
3
Procedure
Using 4-methyl-benzothiazol-2-ylamine and 2-chloronicotinic acid chloride the title compound was obtained as a yellow solid (50% yield), MS: m/e=304 (M+H+).
Sources & evidence
- ORD record
- ord-773ff99f76c4461390ac82d0c2deae89
- Source dataset
- uspto-grants-2008_01
- Patent number
- US07317007B2
Reaction notes
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