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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1895959생성일: 2026년 10월 26일

Benzaldehyde → 2-[3-(1-Benzylpiperidin-4-ylidene)prop-1-ynyl]-6-methylpyridine

https://huagongshe.com/reaction/1895959

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물DichloromethaneHCID 6344—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물2-Methyl-6-(3-piperidin-4-ylideneprop-1-ynyl)pyridineHCID 87550402—
용매WaterHCID 962—
생성물2-[3-(1-Benzylpiperidin-4-ylidene)prop-1-ynyl]-6-methylpyridineHCID 87550713—

반응 단계

A mixture of the compound of Example 3 (0.22 g, 1.04 mmol), benzaldehyde (0.13 mL, 1.25 mmol), sodium triacetoxyborohydride (0.33 g, 1.56 mmol) and 15 mL of CH2Cl2 was stirred overnight at r.t. Afterwards, it was diluted with water, the organic layer was separated, washed with brine (2×15 mL), dried (Na2SO4) and evaporated to dryness in vacuo the give a crude, which was purified by automated flash liquid chromatography (Horizon™-Biotage) eluting with a gradient Petroleum Ether-EtOAc from 85:15 to 0:100 affording the title compound, which was further purified by preparative RP LC-MS chromatography, using MS-C18 XTerra column 30×50 mm eluting with ammonium bicarbonate 20 mM pH 8 buffer-acetonitrile gradient (0.12 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08518916B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-901dddb84a7b4df59e8fc54be1a54a92
출처 메모uspto-grants-2013_08