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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968195Generated: October 25, 2026

Hydrochloric Acid → 2-Amino-5-[(3-carbomethoxyphenyl)thio]thiazole

https://huagongshe.com/reaction/968195

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—
Product2-Amino-5-[(3-carbomethoxyphenyl)thio]thiazoleHCID 2228837175%

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%). B. 3-[[2-[[(1,1-Dimethylethoxy)carbonyl]amino]thiazol-5-yl]thio]benzoic acid methyl ester

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06958336B2
Source datasetuspto-grants-2005_10
ORD IDord-95cb4fb0598f4681829a8390f78d8a55
Source noteuspto-grants-2005_10