4-Morpholinobenzaldehyde → HCID 178521812, compound

HRID 2284213Notes

Reaction equation

[N+:1]([C:4]1[CH:5]=[C:6]([CH:18]=[CH:19][C:20]=1[N+:21]([O-])=O)[NH:7][C:8](=[O:17])[C:9]1[CH:14]=[C:13]([OH:15])[CH:12]=[C:11]([OH:16])[CH:10]=1)([O-])=O.[O:24]1[CH2:29][CH2:28][N:27]([C:30]2[CH:37]=[CH:36][C:33]([CH:34]=O)=[CH:32][CH:31]=2)[CH2:26][CH2:25]1>>[O:24]1[CH2:29][CH2:28][N:27]([C:30]2[CH:37]=[CH:36][C:33]([C:34]3[NH:21][C:20]4[CH:19]=[CH:18][C:6]([NH:7][C:8](=[O:17])[C:9]5[CH:14]=[C:13]([OH:15])[CH:12]=[C:11]([OH:16])[CH:10]=5)=[CH:5][C:4]=4[N:1]=3)=[CH:32][CH:31]=2)[CH2:26][CH2:25]1

Participants

Reactant 2

HCID 2913494-Morpholinobenzaldehyde

HCID 86673989HCID 86673989, compound

Product 1

HCID 178521812HCID 178521812, compound

Procedure

Compound 425 was prepared according to the procedure similar to that described in Scheme III from 3,4-dinitro-N-(3,5-dihydroxybenzoyl)aniline and 4-morpholinobenzaldehyde. [M+H]+ calcd for C24H22N4O4: 431.17; found: 431.18.

Sources & evidence

ORD record: ord-fb5a36e82684459fbfb3c98547f859eb
Source dataset: uspto-grants-2015_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09144557B2

Reaction notes

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