HCID 297403, compound → HCID 137225459, compound

HRID 1031524Notes

Reaction equation

HRID 1031524 reaction equation
[CH3:1][N:2]1[C:6]([NH2:7])=[CH:5][C:4]([CH3:8])=[N:3]1.[CH2:9]([O:11][C:12](=[O:25])[C:13](=[CH:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=1[Cl:24])[C:14]([CH3:16])=O)[CH3:10]>>[ClH:24].[CH2:9]([O:11][C:12]([C:13]1[CH:17]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=2[Cl:24])[C:5]2[C:4]([CH3:8])=[N:3][N:2]([CH3:1])[C:6]=2[NH:7][C:14]=1[CH3:16])=[O:25])[CH3:10]

Participants

3

Reactant 2

HCID 297403HCID 297403, compoundHCID 5207211,3-Dimethyl-1H-pyrazol-5-amine

Product 1

HCID 137225459HCID 137225459, compound

Procedure

Starting from 1,3-dimethyl-5-pyrazolamine and ethyl-2-(2-chlorobenzyliden)acetoacetate. M.p. 240°-242° C.

Sources & evidence

ORD record
ord-31521fc38b6c4876ab9a150f7a57f64a
Source dataset
uspto-grants-1990_09
Patent number
US04954508

Reaction notes

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