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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254684Generated: October 25, 2026

Triethylamine → N-(5-bromothiazol-2-yl)-5-chloro-2-methoxybenzamide

https://huagongshe.com/reaction/254684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Thiazolamine, 5-bromo-HCID 43600—
Reactant5-Chloro-2-methoxybenzoyl chlorideHCID 12384176—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductN-(5-bromothiazol-2-yl)-5-chloro-2-methoxybenzamideHCID 6065487766%

Reaction Steps

To a solution of 2-amino-5-bromothiazole (1220 mg, 6.81 mmol) in dichloromethane (10 ml) was added triethylamine (1.235 ml, 8.86 mmol) and 4-dimethylamino pyridine (83 mg, 0.681 mmol), followed by addition of 5-chloro-2-methoxybenzoyl chloride (1397 mg, 6.81 mmol) and stirred overnight. The reaction was concentrated and water was added to the residue. The mixture was sonicated and filtered to obtain the title compound as off-white solid (1.56 g, 66%). 1H NMR (300 MHz, DMSO-D6) δ ppm 3.88 (m, 3H) 7.23 (d, J=8.81 Hz, 1H) 7.58-7.67 (m, 3H) 12.32 (s, 1H); MS (DCI/NH3) m/z 347 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875640B2
Source datasetuspto-grants-2011_01
ORD IDord-54016b6244354e10b3e7953c0f93d7db
Source noteuspto-grants-2011_01