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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989868Generated: October 30, 2026

Ammonium Chloride → 5-Cyano-7-methylthioimidazo[5,1-b]thiazole

https://huagongshe.com/reaction/989868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactantp-Toluenesulphonyl cyanideHCID 87946—
ReactantHCID 23449208HCID 23449208—
ReactantHCID 178420660HCID 178420660—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product5-Cyano-7-methylthioimidazo[5,1-b]thiazoleHCID 2344922049.1%

Reaction Conditions

Temperature-5 °C

Reaction Steps

A 1 M ethylmagnesium bromide/THF solution (2.0 ml) was added in an argon atmosphere at −40° C. to a solution of 405 mg of 5-iodo-7-methylthioimidazo[5,1-b]thiazole in 12 ml of dry THF. The mixture was stirred at the same temperature for 30 min. p-Toluenesulfonyl cyanide (372 mg) was added thereto. The temperature of the system was raised to −5° C. over a period of one hr. A saturated aqueous ammonium chloride solution was added to the reaction mixture. Ethyl acetate was added thereto, followed by washing with saturated brine. The organic layer was dried over anhydrous magnesium sulfate. The solvent was removed by distillation. The residue was purified by column chromatography on silica gel (dichloromethane:ethyl acetate:hexane=3:1:1) to give 131 mg of 5-cyano-7-methylthioimidazo[5,1-b]thiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458780B1
Source datasetuspto-grants-2002_10
ORD IDord-2e3ad34fde524f83863269ae092ce735
Source noteuspto-grants-2002_10