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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236901Generated: October 29, 2026

Benzoyl chloride → N-(5-Methyl-1,3,4-thiadiazol-2-yl)-N-(propan-2-yl)benzamide

https://huagongshe.com/reaction/236901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
Reactant5-Methyl-N-(propan-2-yl)-1,3,4-thiadiazol-2-amineHCID 544670—
SolventPyridineHCID 1049—
ProductN-(5-Methyl-1,3,4-thiadiazol-2-yl)-N-(propan-2-yl)benzamideHCID 21315328—

Reaction Steps

N-(5-methyl-1,3,4-thiadiazol-2-yl)-1-methylethylamine (5 g, 0.032 mole) in pyridine (100 ml) was treated with benzoyl chloride (4.1 ml). The reaction mixture was stirred and heated to reflux for 51/2 hours. The pyridine was removed under reduced pressure and the residue treated with water and extracted with ether (× 3). The ethereal solution was dried, filtered and evaporated to dryness and the residue recrystallised from ether/petrol ether (40°-60° C.) to give the title compound as a pale yellow crystalline solid m.p. 82.5°-83.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04158659
Source datasetuspto-grants-1979_06
ORD IDord-bac5ca7948ec401794ddfe37ff44d6fe
Source noteuspto-grants-1979_06