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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436443Generated: November 2, 2026

Trichloromethanethiol → 3-(4-Bromophenyl)-5-chloro-1,2,4-thiadiazole

https://huagongshe.com/reaction/1436443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloromethanethiolHCID 6390—
ReactantTriethylamineHCID 8471—
Reactant4-Bromobenzene-1-carboximidamide--hydrogen chloride (1/1)HCID 12207714—
SolventDichloromethaneHCID 6344—
Product3-(4-Bromophenyl)-5-chloro-1,2,4-thiadiazoleHCID 1183264128%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Bromobenzenecarboximidamide hydrochloride (1.00 g, 4.25 mmol), prepared in the previous step, was suspended in methylene chloride (25 mL) and triethylamine (6.1 mL, 42.5 mmol) was added and the mixture was cooled to 0° C. Perchloromethyl mercaptan (0.47 g, 4.25 mmol) was added slowly, the mixture was stirred for 30 min, warmed to 25° C. and stirred 4 h. The mixture was diluted with methylene chloride, filtered through the Celite™ reagent, and concentrated. Flash chromatography (2% acetone in hexane) afforded 3-(4-bromophenyl)-5-chloro-1,2,4-thiadiazole (327 mg, 28%). HRMS: calcd for C8H4BrClN2S, 273.89671; found (EI, M+.), 273.8968; Analytical HPLC: purity 100% at 210-370 nm, 11.2 min; 100% at 272 nm, 11.2 min; the Xterra® RP18 column, 3.5μ, 150×4.6 mm column, 1.2 mL/min, 85/15-5/95 (Ammon. Form. Buff. pH=3.5/ACN+MeOH) for 10 min, hold 4 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618990B2
Source datasetuspto-grants-2009_11
ORD IDord-67a846e3c7184bf68bc721306029be22
Source noteuspto-grants-2009_11