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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68994생성일: 2026년 10월 24일

4-Pyridinecarboxaldehyde → (2-Pyridin-3-ylethyl)pyridin-4-ylmethylamine

https://huagongshe.com/ko/reaction/68994

반응식

참여 물질

역할이름HCID투입량
반응물4-PyridinecarboxaldehydeHCID 13389—
반응물2-(Pyridin-3-yl)ethan-1-amineHCID 854051—
반응물Sodium borohydrideHCID 4311764—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물(2-Pyridin-3-ylethyl)pyridin-4-ylmethylamineHCID 60761584—

반응 단계

4-Pyridine carbaldehyde (5.36 g) and 3-(2-aminoethyl)pyridine (6.5 ml) were added to 100 ml of methanol. The mixture was stirred at room temperature for 7 hours. The mixture was cooled to 0° C., and sodium borohydride (2.8 g) was added thereto. The mixture was further stirred at 0° C. for an hour. Water was added to the reaction mixture and methanol was distilled off under reduced pressure. The residue was subjected to extraction using dichloromethane. The organic layer was washed with saturated saline, dried with anhydrous sodium sulfate, and was condensed under reduced pressure. The residue was purified by basic silica gel column chromatography (ethyl acetate:methanol=95:5→85:5). The purified product was condensed under reduced pressure to give the title compound (10.03 g) as a colorless oily matter.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822453B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-d4f48387114947c59fea3f727a7bc9b3
출처 메모uspto-grants-2014_09