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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 972071Generated: October 29, 2026

Triethylamine → N-Methyl-N-(3-methyl-1,2,4-thiadiazol-5-yl)cyclohexanecarboxamide

https://huagongshe.com/reaction/972071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCyclohexanecarbonyl chlorideHCID 75938—
ReactantN,3-Dimethyl-1,2,4-thiadiazol-5-amineHCID 12725101—
SolventBenzeneHCID 241—
ProductN-Methyl-N-(3-methyl-1,2,4-thiadiazol-5-yl)cyclohexanecarboxamideHCID 20393633—

Reaction Steps

Cyclohexane carboxylic acid chloride (9.92 g, 0.068 mol) was added slowly to a solution of 5-methylamino-3-methyl-1,2,4-thiadiazole (7.0 g, 0.054 mol) in dry benzene containing triethylamine (6.87 g, 0.068 mol) and the mixture heated under reflux for 11/2 hours, cooled and washed with 2N hydrochloric acid, saturated solution sodium hydrogen carbonate and water; dried over magnesium sulphate, filtered and evaporated down to yield yellow oil which crystallised upon standing. This was recrystallised twice from petroleum ether 60°-80° C. to yield off-white crystals of N-(3-methyl-1,2,4-thiadiazol-5-yl)-N-methylcyclohexane carboxamide. Yield 8.23 g, (63.8%), m.p. 96° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04163048
Source datasetuspto-grants-1979_07
ORD IDord-c4d57d57a342484db77c66b8bde9c4ec
Source noteuspto-grants-1979_07