Methyl 2-(2-nitrobenzylidene)acetoacetate → HCID 136404518, compound

HRID 1031531Notes

Reaction equation

HRID 1031531 reaction equation
[CH2:1]([C:5]1[CH:9]=[C:8]([NH2:10])[N:7]([CH3:11])[N:6]=1)[CH2:2][CH2:3][CH3:4].[CH3:12][O:13][C:14](=[O:29])[C:15](=[CH:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=1[N+:26]([O-:28])=[O:27])[C:16]([CH3:18])=O>>[CH3:12][O:13][C:14]([C:15]1[CH:19]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=2[N+:26]([O-:28])=[O:27])[C:9]2[C:5]([CH2:1][CH2:2][CH2:3][CH3:4])=[N:6][N:7]([CH3:11])[C:8]=2[NH:10][C:16]=1[CH3:18])=[O:29]

Participants

3

Reactant 2

HCID 787115Methyl 2-(2-nitrobenzylidene)acetoacetateHCID 13861126HCID 13861126, compound

Product 1

HCID 136404518HCID 136404518, compound

Procedure

Starting from 3-butyl-1-methyl-5-pyrazolamine and methyl-2-(2-nitrobenzyliden)acetoacetate in equimolar proportions.

Sources & evidence

ORD record
ord-2ca1ecb943d54c7a8c7c126df540782b
Source dataset
uspto-grants-1990_09
Patent number
US04954508

Reaction notes

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