4-Morpholinobenzaldehyde → HCID 178522191, compound

HRID 2284126Notes

Reaction equation

[N:1]1([C:7]2[CH:12]=[CH:11][C:10]([NH:13][C:14](=[O:27])[C:15]3[CH:20]=[CH:19][C:18]([N+:21]([O-])=O)=[C:17]([N+:24]([O-])=O)[CH:16]=3)=[CH:9][CH:8]=2)[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.[N:28]1([C:34]2[CH:41]=[CH:40][C:37]([CH:38]=O)=[CH:36][CH:35]=2)[CH2:33][CH2:32][O:31][CH2:30][CH2:29]1>>[O:4]1[CH2:5][CH2:6][N:1]([C:7]2[CH:12]=[CH:11][C:10]([NH:13][C:14]([C:15]3[CH:20]=[CH:19][C:18]4[NH:21][C:38]([C:37]5[CH:36]=[CH:35][C:34]([N:28]6[CH2:33][CH2:32][O:31][CH2:30][CH2:29]6)=[CH:41][CH:40]=5)=[N:24][C:17]=4[CH:16]=3)=[O:27])=[CH:9][CH:8]=2)[CH2:2][CH2:3]1

Participants

Reactant 2

HCID 2913494-Morpholinobenzaldehyde

HCID 87273796HCID 87273796, compound

Product 1

HCID 178522191HCID 178522191, compound

Procedure

Compound 211 was prepared according to the procedure similar to that described in Scheme III from N-(4-morpholinylphenyl)-3,4-dinitrobenzamide and 4-morpholinylbenzaldehyde. [M+H]+ calcd for C28H29N5O3: 484.23; found: 483.92.

Sources & evidence

ORD record: ord-048a92bddecf493ea57a5a12f5ac45f3
Source dataset: uspto-grants-2015_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09144557B2

Reaction notes

Loading…