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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103862Generated: November 2, 2026

5-Methoxycarbonyl-2-thiophenecarboxylic acid hydrazide → methyl 5-[(2-{1-[5-(4-t-butylphenyl)-4-hydroxy-1-methyl-1H-pyrazol-3-yl]ethylidene}hydrazino)carbonyl]-2-thiophenecarboxylate

https://huagongshe.com/reaction/2103862

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methoxycarbonyl-2-thiophenecarboxylic acid hydrazideHCID 14871961—
Reactant1-[5-(4-t-Butylphenyl)-4-hydroxy-1-methyl-1H-pyrazol-3-yl]ethanoneHCID 67050084—
SolventDimethylformamideHCID 6228—
Productmethyl 5-[(2-{1-[5-(4-t-butylphenyl)-4-hydroxy-1-methyl-1H-pyrazol-3-yl]ethylidene}hydrazino)carbonyl]-2-thiophenecarboxylateHCID 7235993031.4%

Reaction Conditions

Temperature110 °C

Reaction Steps

1-[5-(4-t-Butylphenyl)-4-hydroxy-1-methyl-1H-pyrazol-3-yl]ethanone (38.0 mg, 0.14 mmol) and methyl 5-hydrazinocarbonyl-2-thiophenecarboxylate (27.9 mg, 0.14 mmol) were dissolved in dimethylformamide (2.0 mL) and stirred at 110° C. for 12 hours. After cooling, the solvent was evaporated, and ethyl acetate was added to the resulting crude product. The precipitated solid was recovered by filtration to give 20.0 mg of the desired product as a pale yellow solid (yield 31%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576115B2
Source datasetuspto-grants-2009_08
ORD IDord-75cebbc6b7b44682831b1c09639c9916
Source noteuspto-grants-2009_08