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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49136Generated: October 24, 2026

Hydrochloric Acid → 3-[(2-Aminothiazol-5-yl)thio]benzoic acid ethyl ester

https://huagongshe.com/en/reaction/49136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,4-DioxaneHCID 31275—
ReactantBenzoic acid, 3-mercapto-HCID 95737—
ReactantSodium MethoxideHCID 10942334—
Reactant5-Bromo-1,3-thiazol-2-amine--hydrogen chloride (1/1)HCID 22170392—
SolventMethanolHCID 887—
Product3-[(2-Aminothiazol-5-yl)thio]benzoic acid ethyl esterHCID 8675938375%

Reaction Steps

A 4.37 M solution of sodium methoxide in methanol (10 mL, 43.7 mmol) was added dropwise to a stirred suspension of 2-amino-5-bromothiazole hydrochloride (2.16 g, 10 mmol) and 3-carboxythiophenol (1.85 g, 12 mmol) in methanol (75 mL) at 0-5° C. The solution was allowed to warm to rt. for 2 h and a 4 M solution of hydrogen chloride in dioxane (15 mL, 60 mmol) was added. The suspension was stirred at rt. overnight and concentrated. The crude residue was diluted with satd. aqueous sodium bicarbonate solution (50 mL). The precipitated solid was filtered and washed with water (20 mL, 5×) and ether (20 mL, 5×). The solid was filtered and dried in vacuo at 60° C. to obtain the titled compound (1.97 g, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706717B2
Source datasetuspto-grants-2004_03
ORD IDord-8ac3bf7b1da540dd963f8322954ff904
Source noteuspto-grants-2004_03