Benzo(c)(1,2,5)oxadiazole-5-carbaldehyde → HCID 178482809, compound

HRID 2284109Notes

Reaction equation

HRID 2284109 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.[N:25]1[O:29][N:28]=[C:27]2[CH:30]=[C:31]([CH:34]=O)[CH:32]=[CH:33][C:26]=12>>[N:25]1[O:29][N:28]=[C:27]2[CH:30]=[C:31]([C:34]3[NH:22][C:21]4[CH:20]=[CH:19][C:6]([NH:7][C:8](=[O:18])[C:9]5[CH:10]=[CH:11][C:12]([N:15]([CH3:16])[CH3:17])=[CH:13][CH:14]=5)=[CH:5][C:4]=4[N:1]=3)[CH:32]=[CH:33][C:26]=12

Participants

3

Reactant 2

HCID 2776296Benzo(c)(1,2,5)oxadiazole-5-carbaldehydeHCID 86673952HCID 86673952, compound

Product 1

HCID 178482809HCID 178482809, compound

Procedure

Compound 186 was prepared according to the procedure similar to that described in Scheme III from 3,4-dinitro-N-(4-dimethylaminobenzoyl)aniline and benzofurazan-5-carboxaldehyde. [M+H]+ calcd for C22H18N6O2: 399.15; found: 399.47.

Sources & evidence

ORD record
ord-be44e876476f442480b2fb99e64e962c
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

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