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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263349Generated: October 30, 2026

Trichloromethanethiol → 2-(5-Chloro-[1,2,4]thiadiazol-3-yl)-pyridine

https://huagongshe.com/reaction/2263349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloromethanethiolHCID 6390—
ReactantSodium HydroxideHCID 14798—
ReactantPyridine-2-carboximidamide hydrochlorideHCID 12403615—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-(5-Chloro-[1,2,4]thiadiazol-3-yl)-pyridineHCID 4631846542%

Reaction Steps

To a solution of pyridine-2-carboximidamide hydrochloride (2.00 g, 12.7 mmol) and perchloromethyl mercaptan (1.75 ml, 16.3 mmol) in dichloromethane (40 ml) was added dropwise a solution of sodium hydroxide (3.26 g, 81.5 mmol) in water (6 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=2:1) to give 1.05 g (42.0%) of the desired product as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851473B2
Source datasetuspto-grants-2010_12
ORD IDord-b2fd406209c844538e227b437728ce64
Source noteuspto-grants-2010_12