3,4-dinitro-N-(4-morpholinobenzoyl)aniline → HCID 178480753, compound

HRID 2284153Notes

Reaction equation

HRID 2284153 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([NH:13][C:14](=[O:27])[C:15]2[CH:20]=[CH:19][C:18]([N:21]3[CH2:26][CH2:25][O:24][CH2:23][CH2:22]3)=[CH:17][CH:16]=2)[CH:7]=[CH:8][C:9]=1[N+:10]([O-])=O)([O-])=O.[CH3:28][N: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>>[CH3:28][N:29]1[CH2:30][CH2:31][N:32]([C:35]2[CH:36]=[CH:37][C:38]([NH:41][C:42](=[O:43])[C:44]3[CH:45]=[CH:46][C:47]([C:48]4[NH:10][C:9]5[CH:8]=[CH:7][C:6]([NH:13][C:14](=[O:27])[C:15]6[CH:20]=[CH:19][C:18]([N:21]7[CH2:26][CH2:25][O:24][CH2:23][CH2:22]7)=[CH:17][CH:16]=6)=[CH:5][C:4]=5[N:1]=4)=[CH:50][CH:51]=3)=[CH:39][CH:40]=2)[CH2:33][CH2:34]1

Participants

3

Reactant 2

HCID 866739553,4-dinitro-N-(4-morpholinobenzoyl)anilineHCID 866739584-(4-(4-Methylpiperazinyl)phenyl)aminocarbonylbenzaldehyde

Product 1

HCID 178480753HCID 178480753, compound

Procedure

Compound 250 was prepared according to the procedure similar to that described in Scheme III from N-(3,4-dinitrophenyl)-4-morpholinobenzamide and 4-(4-(4-methylpiperazinyl)phenyl)aminocarbonylbenzaldehyde. [M+H]+ calcd for C36H37N7O3: 616.30; found: 616.13.

Sources & evidence

ORD record
ord-f9b4cec104044608a2736dbd9035b2bc
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

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