2,3-Dihydro-1,4-benzodioxin-6-carbaldehyde → HCID 178482807, compound

HRID 2284108Notes

Reaction equation

HRID 2284108 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:30]2[CH:31]=[CH:32][C:33]([CH:35]=O)=[CH:34][C:29]=2[O:28][CH2:27][CH2:26]1>>[O:25]1[CH2:26][CH2:27][O:28][C:29]2[CH:34]=[C:33]([C:35]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:32]=[CH:31][C:30]1=2

Participants

3

Reactant 2

HCID 2481272,3-Dihydro-1,4-benzodioxin-6-carbaldehydeHCID 86673952HCID 86673952, compound

Product 1

HCID 178482807HCID 178482807, compound

Procedure

Compound 184 was prepared according to the procedure similar to that described in Scheme III from 3,4-dinitro-N-(4-dimethylaminobenzoyl)aniline and benzo[1,4]dioxane-6-carboxaldehyde. [M+H]+ calcd for C24H22N4O3: 415.17; found: 415.47.

Sources & evidence

ORD record
ord-9e2554d5392741198a322273dc6aa122
Source dataset
uspto-grants-2015_09
Patent number
US09144557B2

Reaction notes

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