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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1425345생성일: 2026년 10월 27일

Hydrogen chloride-ethyl acetate → Ethyl 2-(3-aminoazetidin-1-yl)-4-methyl-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/1425345

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen chloride-ethyl acetateHCID 21866389—
반응물Ethyl 2-{3-[(tert-butoxycarbonyl)amino]azetidin-1-yl}-4-methyl-1,3-thiazole-5-carboxylateHCID 67549080—
용매1,4-DioxaneHCID 31275—
생성물Ethyl 2-(3-aminoazetidin-1-yl)-4-methyl-1,3-thiazole-5-carboxylateHCID 6754869879.6%

반응 단계

A 4 N hydrochloric acid/ethyl acetate solution (0.96 mL, 3.82 mmol) was added to a solution of ethyl 2-{3-[(tert-butoxycarbonyl)amino]azetidin-1-yl}-4-methyl-1,3-thiazole-5-carboxylate obtained in Example (218a) (261 mg, 0.76 mmol) in 1,4-dioxane (8 mL) at 0° C., and the mixture was stirred at room temperature for 7.5 hours. Then, a 4 N hydrochloric acid/ethyl acetate solution (0.96 mL, 3.82 mmol) was added, and the mixture was further stirred for 45 hours. The reaction solution was concentrated, and saturated aqueous sodium bicarbonate solution was added to the resulting residue. Thereafter, the mixture was extracted with ethyl acetate, and the combined organic layers were dried over anhydrous magnesium sulfate. Following filtration, the solvent was evaporated under reduced pressure to obtain 146 mg of the title compound as a pale yellow oily substance (79%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08927588B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-24974d3efac3472dab6a41486e8ba4c3
출처 메모uspto-grants-2015_01