4-(4-Morpholinophenyl)aminocarbonylbenzaldehyde → HCID 67686866, compound

HRID 2284278Notes

Reaction equation

HRID 2284278 reaction equation
[CH2:1]([N:3]([CH2:19][CH3:20])[CH2:4][CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([N+:13]([O-])=O)=[C:9]([N+:16]([O-])=O)[CH:8]=1)[CH3:2].[O:21]1[CH2:26][CH2:25][N:24]([C:27]2[CH:32]=[CH:31][C:30]([NH:33][C:34]([C:36]3[CH:43]=[CH:42][C:39]([CH:40]=O)=[CH:38][CH:37]=3)=[O:35])=[CH:29][CH:28]=2)[CH2:23][CH2:22]1>>[CH2:1]([N:3]([CH2:19][CH3:20])[CH2:4][CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]2[N:13]=[C:40]([C:39]3[CH:38]=[CH:37][C:36]([C:34]([NH:33][C:30]4[CH:29]=[CH:28][C:27]([N:24]5[CH2:23][CH2:22][O:21][CH2:26][CH2:25]5)=[CH:32][CH:31]=4)=[O:35])=[CH:43][CH:42]=3)[NH:16][C:9]=2[CH:8]=1)[CH3:2]

Participants

3

Procedure

Compound 643 was prepared according to the procedure similar to that described in Scheme III from 1-(2-diethylaminoethyloxy)-3,4-dinitrobenzene and 4-(4-(4-morpholinophenyl)aminocarbonylbenzaldehyde. [M+H]+ calcd for C30H35N5O3: 514.27; found: 514.13.

Sources & evidence

ORD record
ord-dd84f597a0254bd283a82ecbb7ba9678
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

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