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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30452생성일: 2026년 10월 24일

Piperidine → Methyl 6-(piperidin-1-ylmethyl)nicotinate

https://huagongshe.com/ko/reaction/30452

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물Methyl 6-formylpyridine-3-carboxylateHCID 586269—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매DichloromethaneHCID 6344—
용매Sodium HydroxideHCID 14798—
생성물AmmoniaHCID 2221%
생성물Methyl 6-(piperidin-1-ylmethyl)nicotinateHCID 44515770148.2%

반응 단계

To a solution of 6-formyl-nicotinic acid methyl ester (0.200 g, 1.21 mmol) and piperidine (0.14 mL, 1.33 mmol) in DCM (15 mL) was added NaB(OAc)3H (0.380 g, 1.80 mmol). After 18 h, the reaction was diluted with 1 N NaOH (10 mL) and extracted with DCM (2×50 mL). The organic layers were combined, dried (Na2SO4), and concentrated. Chromatography of the residue (SiO2; 1-3% 2 M NH3 in MeOH/DCM) gave the title compound as an oil (0.210 g, 74%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423147B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-0f2d767c6c3c4174915665f9ecb1aee8
출처 메모uspto-grants-2008_09