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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422809Generated: October 31, 2026

5-(hydrazinecarbonyl)-N-(pyridine-4-ylmethyl)thiophene-2-carboxamide → 5-{1-[5-(3,4-dichlorophenyl)-4-hydroxy-1-methyl-1H-pyrazol-3-yl]ethylidenehydrazinocarbonyl}thiophene-2-carboxylic Acid 4-picolylamide

https://huagongshe.com/reaction/2422809

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(hydrazinecarbonyl)-N-(pyridine-4-ylmethyl)thiophene-2-carboxamideHCID 57688144—
Reactant1-[5-(3,4-dichlorophenyl)-4-hydroxy-1-methyl-1H-pyrazol-3-yl]ethanoneHCID 60206780—
SolventDimethyl SulfoxideHCID 679—
Product5-{1-[5-(3,4-dichlorophenyl)-4-hydroxy-1-methyl-1H-pyrazol-3-yl]ethylidenehydrazinocarbonyl}thiophene-2-carboxylic Acid 4-picolylamideHCID 7659784953%

Reaction Steps

1-[5-(3,4-Dichlorophenyl)-4-hydroxy-1-methyl-1H-pyrazol-3-yl]ethanone (40 mg, 0.14 mmol) in dimethyl sulfoxide (1.0 mL) was mixed with 5-hydrazinocarbonylthiophene-2-carboxylic acid 4-picolylamide (39 mg, 0.14 mmol) prepared in Reference Synthetic Example 4 and left at 100° C. for 10.5 hours. The solvent was evaporated, and the residue was dissolved in chloroform (1.0 mL). After addition of n-hexane (2.0 mL), the resulting crystals were recovered by filtration to give 40 mg of the desired product (yield 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960425B2
Source datasetuspto-grants-2011_06
ORD IDord-0ff30061994047c8b0a7446172daecc5
Source noteuspto-grants-2011_06