2,3-Dihydrobenzofuran-5-carboxaldehyde → HCID 178482806, compound

HRID 2284107Notes

Reaction equation

HRID 2284107 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([CH:19]=[CH:20][C:21]=1[N+:22]([O-])=O)[NH:7][C:8](=[O:18])[C:9]1[CH:14]=[CH:13][C:12]([N:15]([CH3:17])[CH3:16])=[CH:11][CH:10]=1)([O-])=O.[O:25]1[C:29]2[CH:30]=[CH:31][C:32]([CH:34]=O)=[CH:33][C:28]=2[CH2:27][CH2:26]1>>[O:25]1[C:29]2[CH:30]=[CH:31][C:32]([C:34]3[NH:22][C:21]4[CH:20]=[CH:19][C:6]([NH:7][C:8](=[O:18])[C:9]5[CH:14]=[CH:13][C:12]([N:15]([CH3:17])[CH3:16])=[CH:11][CH:10]=5)=[CH:5][C:4]=4[N:1]=3)=[CH:33][C:28]=2[CH2:27][CH2:26]1

Participants

3

Reactant 2

HCID 7359012,3-Dihydrobenzofuran-5-carboxaldehydeHCID 86673952HCID 86673952, compound

Product 1

HCID 178482806HCID 178482806, compound

Procedure

Compound 183 was prepared according to the procedure similar to that described in Scheme III from 3,4-dinitro-N-(4-dimethylaminobenzoyl)aniline and 2,3-dihydrobenzofuran-5-carboxaldehyde. [M+H]+ calcd for C24H24N4O2: 399.18; found: 399.47.

Sources & evidence

ORD record
ord-24f1a1a18f2a418eb5bdb8c037c555be
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

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