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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49136생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물1,4-DioxaneHCID 31275—
반응물Benzoic acid, 3-mercapto-HCID 95737—
반응물Sodium MethoxideHCID 10942334—
반응물5-Bromo-1,3-thiazol-2-amine--hydrogen chloride (1/1)HCID 22170392—
용매MethanolHCID 887—
생성물3-[(2-Aminothiazol-5-yl)thio]benzoic acid ethyl esterHCID 8675938375%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706717B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-8ac3bf7b1da540dd963f8322954ff904
출처 메모uspto-grants-2004_03