4-(4-Morpholinophenyl)aminocarbonylbenzaldehyde → HCID 178522197, compound

HRID 2284156Notes

Reaction equation

HRID 2284156 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([CH:22]=[CH:23][C:24]=1[N+:25]([O-])=O)[NH:7][C:8]([C:10]1[CH:11]=[CH:12][C:13]([N:16]2[CH2:21][CH2:20][O:19][CH2:18][CH2:17]2)=[N:14][CH:15]=1)=[O:9])([O-])=O.[N:28]1([C:34]2[CH:39]=[CH:38][C:37]([NH:40][C:41]([C:43]3[CH:50]=[CH:49][C:46]([CH:47]=O)=[CH:45][CH:44]=3)=[O:42])=[CH:36][CH:35]=2)[CH2:33][CH2:32][O:31][CH2:30][CH2:29]1>>[O:19]1[CH2:20][CH2:21][N:16]([C:13]2[CH:12]=[CH:11][C:10]([C:8]([NH:7][C:6]3[CH:22]=[CH:23][C:24]4[NH:25][C:47]([C:46]5[CH:49]=[CH:50][C:43]([C:41](=[O:42])[NH:40][C:37]6[CH:38]=[CH:39][C:34]([N:28]7[CH2:29][CH2:30][O:31][CH2:32][CH2:33]7)=[CH:35][CH:36]=6)=[CH:44][CH:45]=5)=[N:1][C:4]=4[CH:5]=3)=[O:9])=[CH:15][N:14]=2)[CH2:17][CH2:18]1

Participants

3

Reactant 2

HCID 866739754-(4-Morpholinophenyl)aminocarbonylbenzaldehydeHCID 872739073,4-dinitro-N-(2-morpholinyl-5-pyridinecarbonyl)aniline

Product 1

HCID 178522197HCID 178522197, compound

Procedure

Compound 253 was prepared according to the procedure similar to that described in Scheme III from 3,4-dinitro-N-(2-morpholinyl-5-pyridinecarbonyl)aniline and 4-(4-morpholinylphenyl)aminocarbonylbenzaldehyde. [M+H]+ calcd for C34H33N7O4: 604.26; found: 604.10.

Sources & evidence

ORD record
ord-c3f391c1b7b943519117f52764caf96f
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

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