4-(2-Morpholinylethyl)aminocarbonylbenzaldehyde → HCID 178523409, compound

HRID 2284143Notes

Reaction equation

HRID 2284143 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([CH2:33][CH2:34][NH:35][C:36]([C:38]2[CH:45]=[CH:44][C:41]([CH:42]=O)=[CH:40][CH:39]=2)=[O:37])[CH2:32][CH2:31][O:30][CH2:29][CH2:28]1>>[O:30]1[CH2:29][CH2:28][N:27]([CH2:33][CH2:34][NH:35][C:36](=[O:37])[C:38]2[CH:45]=[CH:44][C:41]([C:42]3[NH:10][C:9]4[CH:8]=[CH:7][C:6]([NH:13][C:14](=[O:26])[C:15]5[CH:20]=[CH:19][C:18]([N:21]6[CH2:25][CH2:24][CH2:23][CH2:22]6)=[CH:17][CH:16]=5)=[CH:5][C:4]=4[N:1]=3)=[CH:40][CH:39]=2)[CH2:32][CH2:31]1

Participants

3

Reactant 2

HCID 183630924-(2-Morpholinylethyl)aminocarbonylbenzaldehydeHCID 86673966N-(3,4-dinitrophenyl)-4-pyrrolidinylbenzamide

Product 1

HCID 178523409HCID 178523409, compound

Procedure

Compound 231 was prepared according to the procedure similar to that described in Scheme III from N-(3,4-dinitrophenyl)-4-pyrrolidinylbenzamide and 4-(2-morpholinylethyl)aminocarbonylbenzaldehyde. [M+H]+ calcd for C31H34N6O3: 539.28; found: 539.63.

Sources & evidence

ORD record
ord-ebbac14055ea44518ada32bab070cee3
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

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