돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 555321생성일: 2026년 10월 23일

Hydrochloric Acid → Hydrochloric Acid

https://huagongshe.com/ko/reaction/555321

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium hydrideHCID 24758—
반응물1-CyclohexylpiperazineHCID 87298—
반응물(Oxiran-2-yl)methyl 3-nitrobenzene-1-sulfonateHCID 286836—
반응물3-ChlorocarbazoleHCID 520302—
용매TetrahydrofuranHCID 8028—
생성물Hydrochloric AcidHCID 313—
생성물(+/-)-1-(3-Chlorocarbazol-9-yl)-3-(4-cyclohexylpiperazin-1-yl)propan-2-olHCID 66742182—

반응 조건

온도60 °C

반응 단계

A solution of NaH (0.026 g, 0.60 mmol, 55% in mineral oil) is added into a solution of 3-chloro-9H-carbazole (0.100 g, 0.50 mmol) in anhydrous THF (5 mL). After 30 min of stirring at rt a solution of (±)-3-nitro-benzenesulfonic acid oxiranylmethyl ester in anhydrous THF (0.5 mL) is added. After 90 min of stirring at rt a solution of 1-cyclohexyl piperazine (0.25 g, 1.50 mmol) in anhydrous THF (1 mL) is then added. The resulting mixture is allowed to stir at 60° C. for 15 hours. The reaction mixture is quenched with brine (15 mL) and extracted with Et2O (50 mL+2×25 mL). After drying over MgSO4, evaporation under reduced pressure, the crude compound is purified via flash chromatography on a 3×24 cm2 SiO2 column using EtOAc/MeOH (8/1) and (4/1) as eluant. A solution of the purified above compound (0.088 g, 0.21 mmol, 41%) is treated with HCl (1M in Et2O) to give the title compound hydrochloride (0.085 g, 0.17 mmol) as a white powder in a 34% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08053436B1
출처 데이터셋uspto-grants-2011_11
ORD IDord-4e6860f4b89f4c70b3dd8181fc9e21cc
출처 메모uspto-grants-2011_11