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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 428564생성일: 2026년 10월 23일

Acetic Acid → HCID 178480352, 화합물

https://huagongshe.com/ko/reaction/428564

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물4-(5-fluoro-1-methyl-1H-indol-3-yl)-cyclohexanoneHCID 18414059—
반응물6-Bromo-8-piperazin-1-yl-quinolineHCID 18414063—
용매1,1-DichloroethaneHCID 6365—
생성물HCID 178480352HCID 178480352—

반응 단계

To a solution of 6-bromo-8-piperazin-1-yl-quinoline (610 mg, 2.09 mmol), 4-(5-fluoro-1-methyl-1H-indol-3-yl)-cyclohexanone (510 mg, 2.09 mmol), and sodium triacetoxyborohydride (660 mg, 3.14 mmol) in dichloroethane (40 mL) was added acetic acid (0.24 mL, 4.18 mmol) and stirred overnight at room temperature. The reaction was quenched with 1 M NaOH (50 mL) and H2O (100 mL) then extracted in CH2Cl2 (100 mL) and EtOAc (100 mL). The organic fractions were combined, dried over Na2SO4, concentrated, filtered and chromatographed (5% MeOH/EtOAc). The majority of the cis compound precipitated out of 5% MeOH/EtOAc before application to the column and was purified by filtration affording 510 mg (47%) of the cis isomer as a pale yellow solid: mp 215-217° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06313126B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-80d4d186d76f4258b0f6708d2ff5d583
출처 메모uspto-grants-2001_11