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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728925Generated: November 2, 2026

(4-Chlorophenyl)hydrazine → HCID 19016808, compound

https://huagongshe.com/reaction/1728925

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Chlorophenyl)hydrazineHCID 70624—
ReactantHCID 15225037HCID 15225037—
SolventEthanolHCID 702—
ProductHCID 19016808HCID 1901680840.2%

Reaction Steps

A mixture of 2.4 g of 2-bromo-4-oxo-5,6-dihydro-4H-thieno[2,3-b]thiopyran-5-acetic acid and 1.3 g of 4-chlorophenylhydrazine in 40 ml of ethanol is refluxed under heating for 14 hours. After cooling, the precipitated crystals are collected by filtration, washed with ethanol and then recrystallized from a mixed solvent of chloroform and ethanol to give 1.3 g of 8-bromo-2-(4-chlorophenyl)-4a,5-dihydro-2H-thieno[2',3':2,3]thiopyrano[4,5-c]pyridazin-3(4H)-one as pale brown crystals, melting at 169°-170° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05329016
Source datasetuspto-grants-1994_07
ORD IDord-abdc671d3c3843b0ac84e1f8f2c52b24
Source noteuspto-grants-1994_07