4-(1-Pyrrolidinyl)benzaldehyde → HCID 178521803, compound
Reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([NH:13][C:14](=[O:26])[C:15]2[CH:20]=[CH:19][C:18]([N:21]3[CH2:25][CH2:24][CH2:23][CH2:22]3)=[CH:17][CH:16]=2)[CH:7]=[CH:8][C:9]=1[N+:10]([O-])=O)([O-])=O.[N:27]1([C:32]2[CH:39]=[CH:38][C:35]([CH:36]=O)=[CH:34][CH:33]=2)[CH2:31][CH2:30][CH2:29][CH2:28]1>>[N:21]1([C:18]2[CH:19]=[CH:20][C:15]([C:14]([NH:13][C:6]3[CH:7]=[CH:8][C:9]4[NH:10][C:36]([C:35]5[CH:34]=[CH:33][C:32]([N:27]6[CH2:31][CH2:30][CH2:29][CH2:28]6)=[CH:39][CH:38]=5)=[N:1][C:4]=4[CH:5]=3)=[O:26])=[CH:16][CH:17]=2)[CH2:25][CH2:24][CH2:23][CH2:22]1Participants
3
Procedure
Compound 225 was prepared according to the procedure similar to that described in Scheme III from N-(3,4-dinitrophenyl)-4-pyrrolidinylbenzamide and 4-pyrrolidinylbenzaldehyde. [M+H]+ calcd for C28H29N5O: 452.25; found: 451.95.
Sources & evidence
- ORD record
- ord-84300bf5e6c04c1d9105b90f2dd1625f
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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