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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 47529생성일: 2026년 10월 24일

1-Acetoxy-2-bromoethane → 1-[1-(1-methoxycarbonylpiperidin-4-yl)-piperidin-4-yl]-3-(2-acetoxy-ethyl)-1,3-dihydro-2H-benzimidazol-2-one

https://huagongshe.com/ko/reaction/47529

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참여 물질

역할이름HCID투입량
반응물1-Acetoxy-2-bromoethaneHCID 13564—
반응물Sodium hydrideHCID 24758—
반응물1-[1-(1-methoxycarbonylpiperidin-4-yl)piperidin-4-yl]-1,3-dihydro-2H-benzimidazol-2-oneHCID 22745218—
용매TetrahydrofuranHCID 8028—
생성물1-[1-(1-methoxycarbonylpiperidin-4-yl)-piperidin-4-yl]-3-(2-acetoxy-ethyl)-1,3-dihydro-2H-benzimidazol-2-oneHCID 22745243—

반응 조건

온도40 °C

반응 단계

Three-hundred (300) mg of 1-[1-(1-methoxycarbonylpiperidin-4-yl)piperidin-4-yl]-1,3-dihydro-2H-benzimidazol-2-one was dissolved in 15 ml of tetrahydrofuran, and to which 33 mg of 60% sodium hydride was added. After evolution of a gas ceased, 93 μl of (2-bromoethyl)acetate was added, heated to 40° C. and stirred for 2 hours. The reaction liquid was concentrated and the remaining matter was distributed between water and chloroform. The chloroform layer was separated, dried over anhydrous sodium sulfate, concentrated and the residue was purified by silica gel column chromatography (chloroform/methanol=19/1). Thus 354 mg of 1-[1-(1-methoxycarbonylpiperidin-4-yl)-piperidin-4-yl]-3-(2-acetoxy-ethyl)-1,3-dihydro-2H-benzimidazol-2-one was obtained. The product was dissolved in 10 ml of methanol, to which 35 mg of sodium borohydride was added and stirred for 7 hours at room temperature. The reaction liquid was concentrated, to which water was added and extracted with chloroform. The chloroform layer was dried over anhydrous sodium sulfate and then concentrated. The residue was purified by silica gel column chromatography (chloroform/methanol=19/1), to provide 246 mg of the title compound as a colorless, amorphous substance.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06699880B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-e8d4d9656f5d4a12bcb5a503bca60382
출처 메모uspto-grants-2004_03