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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702636Generated: November 1, 2026

Pyridine → HCID 15580737, compound

https://huagongshe.com/reaction/1702636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantHCID 15580707HCID 15580707—
SolventWaterHCID 962—
ProductHCID 15580737HCID 15580737—

Reaction Steps

A stirred mixture of 2.30 g. of 3-amino-1-(3,4-dichlorophenyl)-2-pyrazoline (prepared as described in Example 1) in 20 ml. of dry pyridine is cooled in an ice bath, then 2.10 g. of p-chlorobenzoyl chloride is added. The reaction mixture is allowed to stand at room temperature for 16 hours then is poured into water to separate a solid. The solid is collected by filtration and dissolved in dichloromethane. This solution is passed through a short column of a hydrous magnesium silicate. The effluent is refluxed and hexane is added until turbidity results. The solution is cooled and filtered to collect a product. The product is recrystallized from the same solvent pair to give 1.8 g. of the desired product as yellow needles, m.p. 177°-178° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04348527
Source datasetuspto-grants-1982_09
ORD IDord-e086e80b452b46bf9ab919a58684704c
Source noteuspto-grants-1982_09