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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1012912생성일: 2026년 10월 25일

Water → [4-(Benzothiazole-2-carbonyl)-cyclohexyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1012912

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물BenzothiazoleHCID 7222—
반응물ButyllithiumHCID 178418339—
반응물HCID 178502731HCID 178502731—
용매TetrahydrofuranHCID 8028—
생성물[4-(Benzothiazole-2-carbonyl)-cyclohexyl]-carbamic acid tert-butyl esterHCID 6731716682.1%

반응 단계

To a solution of benzothiazole (675 mg, 0.55 ml, 5 mmol) in THF (20 ml) at −78° C. was added dropwise n-BuLi (2.5M in Hex, 2 ml) such that the temperature did not exceed −70° C. The brown solution was stirred at this temperature for 15 min before dropwise addition of a solution of [trans-4-(methoxy-methyl-carbamoyl)-cyclohexyl]-carbamic acid tert-butyl ester (716 mg, 2.5 mmol, prepared according to WO 03/053933) in THF (2 ml). The temperature was kept below −70° C. The brown solution was then gradually allowed to reach RT (over 3 h). Mixture was poured into water and extracted with EtOAc. The combined organic extracts were washed with brine and dried over MgSO4 and concentrated under reduced pressure. The residue was purified by chromatography over SiO2 (Hex/EtOAc 4:1 then DCM). The relevant fractions were pooled, evaporated under reduced pressure, digested with Hex and filtered to give 740 mg (82%) of [4-(benzothiazole-2-carbonyl)-cyclohexyl]-carbamic acid tert-butyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07981886B2
출처 데이터셋uspto-grants-2011_07
ORD IDord-35a01e6be0c24725a8d37793c2468181
출처 메모uspto-grants-2011_07