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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263005Generated: October 29, 2026

Trichloromethanethiol → 5-Chloro-3-(pyrrolidin-1-yl)-1,2,4-thiadiazole

https://huagongshe.com/reaction/2263005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloromethanethiolHCID 6390—
ReactantSodium HydroxideHCID 14798—
ReactantPyrrolidine-1-carboximidamide hydrochlorideHCID 13221241—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product5-Chloro-3-(pyrrolidin-1-yl)-1,2,4-thiadiazoleHCID 6526867931.1%

Reaction Steps

To a solution of pyrrolidine-1-carboximidamide hydrochloride (1.50 g, 10.0 mmol) and perchloromethyl mercaptan (1.08 ml, 10.0 mmol) in dichloromethane (20 ml) was added dropwise a solution of sodium hydroxide (1.60 g, 40.0 mmol) in water (4 ml) under ice-cooling. Then, the reaction mixture was stirred under ice-cooling for 1 hour and at room temperature for 1 hour. The organic layer was separated, washed with water, and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1) to give 590 mg (31.0%) of the desired product as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851473B2
Source datasetuspto-grants-2010_12
ORD IDord-85eba6a90ff84b1eb5ac24e6513fb642
Source noteuspto-grants-2010_12