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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037919Generated: October 26, 2026

1-Hydroxybenzotriazole → 5-chloro-N-(5-chlorothiazol-2-yl)-2-methoxybenzamide

https://huagongshe.com/reaction/1037919

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant5-Chloro-o-anisic acidHCID 76970—
Reactant2-Amino-5-chlorothiazole hydrochlorideHCID 148743—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
Product5-chloro-N-(5-chlorothiazol-2-yl)-2-methoxybenzamideHCID 86618912—

Reaction Steps

A mixture of 2-amino-5-chlorothiazole hydrochloric acid (1.0 g, 5.9 mmol), 5-chloro-2-methoxybenzoic acid (1.3 g, 7.0 mmol), 1-ethyl-(3-dimethylaminopropyl)carbodiimide hydrochloride (Chem-Impex International, 2.2 g, 12 mmol), 1-hydroxybenzotriazole (0.95 g, 7.0 mmol) and 4-dimethylaminopyridine (0.14 g, 1.2 mmol) in 6 mL of pyridine was allowed to stir at ambient temperature for 72 hours. The reaction mixture was concentrated under reduced pressure and 10 mL of H2O was added. The resulting solids were isolated by filtration, washed with 5 mL of H2O and twice with 5 mL of ethyl acetate, and dried to afford the title compound. MS (DCI/NH3) m/Z 303 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546583B2
Source datasetuspto-grants-2013_10
ORD IDord-1943ce5adf034eb19856b210091f4741
Source noteuspto-grants-2013_10