4-Morpholinobenzaldehyde → HCID 178521809, compound

HRID 2284215Notes

Reaction equation

[N+:1]([C:4]1[CH:5]=[C:6]([CH:17]=[CH:18][C:19]=1[N+:20]([O-])=O)[NH:7][C:8](=[O:16])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[OH:15])([O-])=O.[O:23]1[CH2:28][CH2:27][N:26]([C:29]2[CH:36]=[CH:35][C:32]([CH:33]=O)=[CH:31][CH:30]=2)[CH2:25][CH2:24]1>>[O:23]1[CH2:28][CH2:27][N:26]([C:29]2[CH:36]=[CH:35][C:32]([C:33]3[NH:20][C:19]4[CH:18]=[CH:17][C:6]([NH:7][C:8](=[O:16])[C:9]5[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=5[OH:15])=[CH:5][C:4]=4[N:1]=3)=[CH:31][CH:30]=2)[CH2:25][CH2:24]1

Participants

Reactant 2

HCID 2913494-Morpholinobenzaldehyde

HCID 86673991HCID 86673991, compound

Product 1

HCID 178521809HCID 178521809, compound

Procedure

Compound 427 was prepared according to the procedure similar to that described in Scheme III from 3,4-dinitro-N-(2-hydroxybenzoyl)aniline and 4-morpholinobenzaldehyde. [M+H]+ calcd for C24H22N4O3: 415.18; found: 414.98.

Sources & evidence

ORD record: ord-a8d167916e174226a2dd596df4358e07
Source dataset: uspto-grants-2015_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09144557B2

Reaction notes

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