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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263348Generated: November 2, 2026

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

https://huagongshe.com/reaction/2263348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloromethanethiolHCID 6390—
ReactantSodium HydroxideHCID 14798—
ReactantNicotinamidine hydrochlorideHCID 202042—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product3-(5-Chloro-[1,2,4]thiadiazol-3-yl)-pyridineHCID 463184664.4%

Reaction Steps

To a solution of pyridine-3-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=1:1) to give 110 mg (4.38%) of the desired product as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851473B2
Source datasetuspto-grants-2010_12
ORD IDord-fd7f9eb52a4140d984b87d9ac77725d5
Source noteuspto-grants-2010_12