3-Methylbenzo(b)thiophene-2-carboxaldehyde → HCID 66913757, compound
Reaction equation
[CH2:1]([C:8]1[CH:9]=[N:10][C:11]2[C:16]([C:17]=1[C:18]1[CH:19]=[C:20]([NH2:24])[CH:21]=[CH:22][CH:23]=1)=[CH:15][CH:14]=[CH:13][C:12]=2[C:25]([F:28])([F:27])[F:26])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:29][C:30]1[C:31]2[CH:40]=[CH:39][CH:38]=[CH:37][C:32]=2[S:33][C:34]=1[CH:35]=O>>[CH2:1]([C:8]1[CH:9]=[N:10][C:11]2[C:16]([C:17]=1[C:18]1[CH:19]=[C:20]([NH:24][CH2:35][C:34]3[S:33][C:32]4[CH:37]=[CH:38][CH:39]=[CH:40][C:31]=4[C:30]=3[CH3:29])[CH:21]=[CH:22][CH:23]=1)=[CH:15][CH:14]=[CH:13][C:12]=2[C:25]([F:28])([F:26])[F:27])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
This compound was prepared according to the procedure of example 66, substituting 3-(3-benzyl-8-trifluoromethyl-quinolin-4-yl)-phenylamine and 3-methyl benzo[b]thiophene-2-carbaldehyde. MS (ESI) m/z 539.
Workup
- customThis compound was prepared
Sources & evidence
- ORD record
- ord-843749b0f79b41bdadbdd3e65efd67ea
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07576215B2
Reaction notes
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