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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462238Generated: October 25, 2026

Cyclohexylamine → 2-(2-Cyclohexylamino-5-thiadiazolyl)-1-methyl-5nitroimidazole

https://huagongshe.com/reaction/462238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
Reactant2-(2-Chloro-5-thiadiazolyl)-1-methyl-5-nitroimidazoleHCID 21390801—
Solvent1,4-DioxaneHCID 31275—
Product2-(2-Cyclohexylamino-5-thiadiazolyl)-1-methyl-5nitroimidazoleHCID 21390861—

Reaction Steps

A mixture of 5.0 g. of 2-(2-chloro-5-thiadiazolyl)-1-methyl-5-nitroimidazole, 6.0 g. of cyclohexylamine and 125 ml. of dioxane is stirred at reflux until thin-layer chromatographic analysis indicates that the chloro intermediate is completely utilized. The dioxane is removed under reduced pressure and the residue triturated with aqueous sodium bicarbonate solution. Recrystallization from a mixture of ethylacetate and acetone yields the pure compound melting at 215°-217° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04065567
Source datasetuspto-grants-1977_12
ORD IDord-adcb9dcdcc804a23b2b12019b726ef8a
Source noteuspto-grants-1977_12