4-(2-Oxopyrrolidin-1-yl)benzoic acid → HCID 59401761, compound
Reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([N:8]2[CH2:12][CH2:11][CH:10]([N:13]3[CH2:17][CH2:16][CH2:15][CH:14]3[CH3:18])[CH2:9]2)[CH:5]=[CH:4][C:3]=1[NH2:19].[O:20]=[C:21]1[CH2:25][CH2:24][CH2:23][N:22]1[C:26]1[CH:34]=[CH:33][C:29]([C:30](O)=[O:31])=[CH:28][CH:27]=1>>[CH3:1][C:2]1[CH:7]=[C:6]([N:8]2[CH2:12][CH2:11][CH:10]([N:13]3[CH2:17][CH2:16][CH2:15][CH:14]3[CH3:18])[CH2:9]2)[CH:5]=[CH:4][C:3]=1[NH:19][C:30](=[O:31])[C:29]1[CH:28]=[CH:27][C:26]([N:22]2[CH2:23][CH2:24][CH2:25][C:21]2=[O:20])=[CH:34][CH:33]=1Participants
3
Procedure
The title compound was prepared in a manner substantially the same as example 1 by coupling 2-methyl-4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-phenylamine with 4-(2-oxo-pyrrolidin-1-yl)-benzoic acid. MS: 447.5 (M+H).
Sources & evidence
- ORD record
- ord-4ac2539d6b7048129701b2e7d21c9eea
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08618159B2
Reaction notes
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