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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921302Generated: October 26, 2026

Triethylamine → N-(5-tert-butyl-1,3,4-thiadiazol-2-yl)-5-chloro-2-methoxybenzamide

https://huagongshe.com/reaction/1921302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantButhidazolamineHCID 170170—
Reactant5-Chloro-2-methoxybenzoyl chlorideHCID 12384176—
SolventDichloromethaneHCID 6344—
ProductN-(5-tert-butyl-1,3,4-thiadiazol-2-yl)-5-chloro-2-methoxybenzamideHCID 291480498.2%

Reaction Steps

To a solution of 5-tert-butyl-1,3,4-thiadiazol-2-amine (1.57 g, 10 mmol) and 5-chloro-2-methoxybenzoyl chloride (2.05 g, 10 mmol) in CH2Cl2 (45 mL) at 0° C. was added dropwise triethylamine (1.7 mL, 12 mmol) and the reaction mixture was allowed to warm to ambient temperature for 12 h. The mixture was then washed with water, brine, dried with MgSO4, filtered, and concentrated under reduced pressure to afford 3.2 g of the title compound. 1H NMR (300 MHz, DMSO-D6) δ ppm 1.43 (s, 9H), 3.88 (s, 3H), 7.22 (d, J=8.8 Hz, 1H), 7.45-7.76 (m, 2H), 12.43 (s, 1H). MS (DCI/NH3) m/z 326 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173687B2
Source datasetuspto-grants-2012_05
ORD IDord-c65e82761ea04367901f7256a754b519
Source noteuspto-grants-2012_05