4-Formyl-N-(2-hydroxyethyl)benzamide → HCID 178523438, 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.[OH:27][CH2:28][CH2:29][NH:30][C:31]([C:33]1[CH:40]=[CH:39][C:36]([CH:37]=O)=[CH:35][CH:34]=1)=[O:32]>>[OH:27][CH2:28][CH2:29][NH:30][C:31](=[O:32])[C:33]1[CH:40]=[CH:39][C:36]([C:37]2[NH:10][C:9]3[CH:8]=[CH:7][C:6]([NH:13][C:14](=[O:26])[C:15]4[CH:20]=[CH:19][C:18]([N:21]5[CH2:25][CH2:24][CH2:23][CH2:22]5)=[CH:17][CH:16]=4)=[CH:5][C:4]=3[N:1]=2)=[CH:35][CH:34]=1Participants
3
Procedure
Compound 227 was prepared according to the procedure similar to that described in Scheme III from N-(3,4-dinitrophenyl)-4-pyrrolidinylbenzamide and 4-(2-hydroxyethyl)aminocarbonylbenzaldehyde. [M+H]+ calcd for C27H27N5O3: 470.22; found: 469.58.
Sources & evidence
- ORD record
- ord-3ca37a310b0346d88da7c69101779004
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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