N-(3,4-dinitrophenyl)-4-pyrrolidinylbenzamide → HCID 178522202, compound

HRID 2284149Notes

Reaction equation

HRID 2284149 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[CH:32]=[CH:31][CH:30]=[C:29]([NH:33][C:34]([C:36]2[CH:43]=[CH:42][C:39]([CH:40]=O)=[CH:38][CH:37]=2)=[O:35])[CH:28]=1>>[N:27]1[CH:32]=[CH:31][CH:30]=[C:29]([NH:33][C:34](=[O:35])[C:36]2[CH:37]=[CH:38][C:39]([C:40]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:42][CH:43]=2)[CH:28]=1

Participants

3

Reactant 2

HCID 86673966N-(3,4-dinitrophenyl)-4-pyrrolidinylbenzamideHCID 86673974HCID 86673974, compound

Product 1

HCID 178522202HCID 178522202, compound

Procedure

Compound 241 was prepared according to the procedure similar to that described in Scheme III from N-(3,4-dinitrophenyl)-4-pyrrolidinylbenzamide and 4-(3-pyridinylaminocarbonyl)benzaldehyde. [M+H]+ calcd for C30H26N6O2: 503.22; found: 502.97.

Sources & evidence

ORD record
ord-4fad3e044e3c4fa7948a59a2648f6206
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

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