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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576101Generated: November 2, 2026

Chloroform → 2-(Furan-3-yl)imidazo[1,2-b][1,2,4]thiadiazole

https://huagongshe.com/reaction/1576101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantSulfuryl chlorideHCID 24648—
ReactantHCID 54451730HCID 54451730—
SolventMethanolHCID 887—
Product2-(Furan-3-yl)imidazo[1,2-b][1,2,4]thiadiazoleHCID 21514383—

Reaction Steps

To 0.2 g. of 2-(3-furylthiocarbonylamino)-imidazole [(IV), R = 3-furyl] in 10 ml. of chloroform, at 20°-25°C, there is added dropwise 0.1 ml. of sulfuryl chloride in 2 ml. of chloroform. After 10 minutes the reaction mixture is concentrated at 10°-20°C. under vacuum to give a residue which is treated with methanol and filtered. The residue obtained following filtration is treated with dilute aqueous ammonia to give a precipitate which is filtered and dried to yield 2-(3-furyl)-1,2,4-thiadiazolo-[2,3-a]-imidazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03979404
Source datasetuspto-grants-1976_09
ORD IDord-9fcb33bfe83c4566bc75027d7845c545
Source noteuspto-grants-1976_09