N-(3,4-dinitrophenyl)-4-(4-methylpiperazinyl)benzamide → HCID 178480674, compound

HRID 2284152Notes

Reaction equation

HRID 2284152 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([NH:13][C:14](=[O:28])[C:15]2[CH:20]=[CH:19][C:18]([N:21]3[CH2:26][CH2:25][N:24]([CH3:27])[CH2:23][CH2:22]3)=[CH:17][CH:16]=2)[CH:7]=[CH:8][C:9]=1[N+:10]([O-])=O)([O-])=O.[O:29]1[CH2:34][CH2:33][N:32]([C:35]2[CH:40]=[CH:39][C:38]([NH:41][C:42]([C:44]3[CH:51]=[CH:50][C:47]([CH:48]=O)=[CH:46][CH:45]=3)=[O:43])=[CH:37][CH:36]=2)[CH2:31][CH2:30]1>>[CH3:27][N:24]1[CH2:25][CH2:26][N:21]([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:48]([C:47]5[CH:50]=[CH:51][C:44]([C:42](=[O:43])[NH:41][C:38]6[CH:39]=[CH:40][C:35]([N:32]7[CH2:31][CH2:30][O:29][CH2:34][CH2:33]7)=[CH:36][CH:37]=6)=[CH:45][CH:46]=5)=[N:1][C:4]=4[CH:5]=3)=[O:28])=[CH:16][CH:17]=2)[CH2:22][CH2:23]1

Participants

3

Reactant 2

HCID 86673957N-(3,4-dinitrophenyl)-4-(4-methylpiperazinyl)benzamideHCID 866739754-(4-Morpholinophenyl)aminocarbonylbenzaldehyde

Product 1

HCID 178480674HCID 178480674, compound

Procedure

Compound 249 was prepared according to the procedure similar to that described in Scheme III from N-(3,4-dinitrophenyl)-4-(4-methylpiperazinyl)benzamide and 4-(4-morpholinophenyl)aminocarbonylbenzaldehyde. [M+H]+ calcd for C36H37N7O3: 616.30; found: 616.09.

Sources & evidence

ORD record
ord-cce6acab0e524a1e9c083261d7b7288a
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

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