4-Morpholinobenzaldehyde → HCID 178521808, compound

HRID 2284157Notes

Reaction equation

HRID 2284157 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([CH:16]=[CH:17][C:18]=1[N+:19]([O-])=O)[NH:7][C:8](=[O:15])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)([O-])=O.[N:22]1([C:28]2[CH:35]=[CH:34][C:31]([CH:32]=O)=[CH:30][CH:29]=2)[CH2:27][CH2:26][O:25][CH2:24][CH2:23]1>>[O:25]1[CH2:26][CH2:27][N:22]([C:28]2[CH:35]=[CH:34][C:31]([C:32]3[NH:19][C:18]4[CH:17]=[CH:16][C:6]([NH:7][C:8](=[O:15])[C:9]5[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=5)=[CH:5][C:4]=4[N:1]=3)=[CH:30][CH:29]=2)[CH2:23][CH2:24]1

Participants

3

Reactant 2

HCID 2913494-MorpholinobenzaldehydeHCID 15599063HCID 15599063, compound

Product 1

HCID 178521808HCID 178521808, compound

Procedure

Compound 259 was prepared according to the procedure similar to that described in Scheme III from 3,4-dinitro-N-benzoylaniline and 4-morpholinylbenzaldehyde. [M+H]+ calcd for C24H22N4O2: 399.18; found: 398.99.

Sources & evidence

ORD record
ord-09f54ab492b44073956cd40503e0e53b
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

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