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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263353Generated: November 1, 2026

Trichloromethanethiol → Tert-butyl 4-(5-chloro-1,2,4-thiadiazol-3-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2263353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloromethanethiolHCID 6390—
ReactantSodium HydroxideHCID 14798—
ReactantTert-butyl 4-carbamimidoylpiperazine-1-carboxylateHCID 15197650—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(5-chloro-1,2,4-thiadiazol-3-yl)piperazine-1-carboxylateHCID 6652369559.6%

Reaction Steps

To a solution of tert-butyl 4-[amino(imino)methyl]piperazine-1-carboxylate (1.50 g, 5.67 mmol) and perchloromethyl mercaptan (0.609 ml, 5.67 mmol) in dichloromethane (20 ml) was added dropwise a solution of sodium hydroxide (0.907 g, 22.7 mmol) in water (2.5 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 1.03 g (59.5%) of the desired product as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851473B2
Source datasetuspto-grants-2010_12
ORD IDord-457bab2709b24d4496d234e6ab42e904
Source noteuspto-grants-2010_12