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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16596생성일: 2026년 10월 23일

tert-Butyl acrylate → tert-butyl 3-[4-({[(3-isopropyl-2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)carbonyl]amino}methyl)piperidin-1-yl]propanoate

https://huagongshe.com/ko/reaction/16596

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl acrylateHCID 15458—
반응물3-isopropyl-2-oxo-N-(piperidin-4-ylmethyl)-2,3-dihydro-1H-benzimidazole-1-carboxamideHCID 44249188—
용매TetrahydrofuranHCID 8028—
용매Sodium BicarbonateHCID 516892—
생성물tert-butyl 3-[4-({[(3-isopropyl-2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)carbonyl]amino}methyl)piperidin-1-yl]propanoateHCID 6858576016%

반응 단계

A mixture of 3-isopropyl-2-oxo-N-(piperidin-4-ylmethyl)-2,3-dihydro-1H-benzimidazole-1-carboxamide (0.50 g, 1.58 mmol, Step 2), tert-butyl acrylate (0.340 mL, 2.37 mmol) and iPrNEt (0.275 mL, 2.37 mmol) in THF (20 mL) was refluxed for 18 h. After cooling, the reaction mixture was diluted with sat. NaHCO3 aq. (100 mL), extracted with CH2Cl2 (100 mL) for three times. The combined extracts were dried over Na2SO4, filtered and concentrated. The residue was chromatographed on a column of silica gel eluted with MeOH/CH2Cl2 (1:20→1:10) and then NH-silica gel eluted with EtOAc/hexane (1:5→1:2) to give 0.111 g (16%) of title compound as colorless syrup.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737163B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-0f9e13c6d3304deea6cdd84e880c7264
출처 메모uspto-grants-2010_06