5-Benzothiazolamine, 2-methyl- → HCID 25070100, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[N:7]1[C:11]2=[N:12][CH:13]=[CH:14][CH:15]=[C:10]2[CH:9]=[C:8]1[C:16]([O:18]CC)=O.[NH2:21][C:22]1[CH:23]=[CH:24][C:25]2[S:29][C:28]([CH3:30])=[N:27][C:26]=2[CH:31]=1>>[CH3:30][C:28]1[S:29][C:25]2[CH:24]=[CH:23][C:22]([NH:21][C:16]([C:8]3[N:7]([C:2]4[CH:3]=[CH:4][CH:5]=[CH:6][N:1]=4)[C:11]4=[N:12][CH:13]=[CH:14][CH:15]=[C:10]4[CH:9]=3)=[O:18])=[CH:31][C:26]=2[N:27]=1Participants
3
Procedure
This compound was prepared according to the experimental protocol described in Example 6.2, starting with ethyl 1-(2-pyridyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylate obtained according to the protocol described in step 8.1 and 5-amino-2-methylbenzothiazole. A white solid is obtained.
Workup
- customThis compound was prepared
- customobtained
- customA white solid is obtained
Sources & evidence
- ORD record
- ord-ea5a339a18f34069bb188795356f9ece
- Source dataset
- uspto-grants-2011_10
- Patent number
- US08044066B2
Reaction notes
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