HCID 13861126, compound → HCID 136404517, compound

HRID 1031530Notes

Reaction equation

HRID 1031530 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][CH2:14][CH2:15][O:16][C:17](=[O:32])[C:18](=[CH:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=1[N+:29]([O-:31])=[O:30])[C:19]([CH3:21])=O>>[CH3:12][O:13][CH2:14][CH2:15][O:16][C:17]([C:18]1[CH:22]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=2[N+:29]([O-:31])=[O:30])[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:19]=1[CH3:21])=[O:32]

Participants

3

Procedure

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

Sources & evidence

ORD record
ord-93341a4a95e34fae85bad0eceec5c9e2
Source dataset
uspto-grants-1990_09
Patent number
US04954508

Reaction notes

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