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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103868Generated: November 1, 2026

Hydrochloric Acid → 4-{[(2-{[5-(3,4-Dichlorophenyl)-4-hydroxy-3-thienyl]methylene}hydrazino)carbonothioyl]amino}benzoic acid

https://huagongshe.com/reaction/2103868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
Reactant4-(4-Carboxyphenyl)-3-thiosemicarbazideHCID 2757378—
Reactant5-(3,4-Dichlorophenyl)-4-hydroxythiophene-3-carbaldehydeHCID 84819479—
SolventWaterHCID 962—
Product4-{[(2-{[5-(3,4-Dichlorophenyl)-4-hydroxy-3-thienyl]methylene}hydrazino)carbonothioyl]amino}benzoic acidHCID 7236004465.5%

Reaction Steps

2-(3,4-Dichlorophenyl)-3-hydroxy-4-formylthiophene (52 mg, 0.19 mmol) synthesized in Reference Synthetic Example 26 and 4-hydrazinocarbonothioylaminobenzoic acid (40 mg, 0.19 mmol) were stirred with dimethylformamide (1.9 mL) and concentrated hydrochloric acid (0.1 mL) at room temperature for 14 hours. Water was added to the reaction solution, and the precipitated solid was recovered by filtration and dried. The crude product was stirred with chloroform at room temperature and recovered by filtration to give the desired product as a pale yellow solid (58 mg, yield 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576115B2
Source datasetuspto-grants-2009_08
ORD IDord-d205f4416e0c4451a4c3f2709bae9919
Source noteuspto-grants-2009_08