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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 520487생성일: 2026년 10월 24일

Ethyl 2-((tert-butoxycarbonyl)amino)-1,3-thiazole-4-carboxylate → (4-Hydroxymethylthiazol-2-yl)carbamic acid tert-butyl ester

https://huagongshe.com/ko/reaction/520487

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl 2-((tert-butoxycarbonyl)amino)-1,3-thiazole-4-carboxylateHCID 22280595—
반응물Lithium triethylborohydrideHCID 23712863—
용매TetrahydrofuranHCID 8028—
용매Acetonitrile dry iceHCID 86587134—
생성물(4-Hydroxymethylthiazol-2-yl)carbamic acid tert-butyl esterHCID 2228047572%

반응 조건

온도-45 °C

반응 단계

Ethyl 2-(tert-butoxycarbonylamino)thiazole-4-carboxylate 88 (10.5 g, 38.6 mmol) was dissolved in 300 mL of anhydrous THF and cooled in dry ice-acetonitrile bath. A solution of 1 M Super Hydride™ in THF (85 mL) was then added over a period of 10 min. The resulting reaction mixture was stirred at −45° C. for 2 h. Another portion of 1 M Super Hydride™ in THF (35 mL) was then added and the reaction mixture was stirred for an additional 2 h at −45° C. The reaction was quenched at −45° C. by the addition of 50 mL of brine. Upon warming to room temperature, the reaction mixture was concentrated under reduced pressure. The resulting mixture was extracted with EtOAc. The combined organic layers were washed with brine, dried with Na2SO4, and concentrated under reduced pressure. The resulting residue was purified by chromatography to afford 89 (6.39 g, 72% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09326986B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-10a357909e524ca49f2be272cb2ef0ee
출처 메모uspto-grants-2016_05