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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 327418생성일: 2026년 10월 25일

Acetic Acid → 6-[4-(3,6-Dihydro-4-phenyl-1(2H)-pyridinyl)-1-butynyl]-N-propyl-3-pyridinamine

https://huagongshe.com/reaction/327418

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물PropanalHCID 527—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물6-[4-(3,6-Dihydro-4-phenyl-1(2H)-pyridinyl)-1-butynyl]-3-pyridinamineHCID 10086348—
용매1,1-DichloroethaneHCID 6365—
생성물6-[4-(3,6-Dihydro-4-phenyl-1(2H)-pyridinyl)-1-butynyl]-N-propyl-3-pyridinamineHCID 19960149—

반응 단계

A solution of propionaldehyde (0.18 mL, 2.5 mmol), 6-[4-(3,6-dihydro-4-phenyl-1(2H)-pyridinyl)-1-butynyl]-3-pyridinamine (Example 13) (0.83 g, 2.7 mmoL) and glacial acetic acid (0.14 mL, 2.5 mmol) in 20 mL of dichloroethane is treated with sodium triacetoxyborohydride (0.79 g, 3.7 mmol) under nitrogen and is stirred at room temperature for 18 hours. The reaction is quenched with saturated aqueous sodium bicarbonate, diluted with dichloromethane, and the organic layer is dried (sodium sulfate) and concentrated under reduced pressure. The residue is chromatographed (silica gel, 1% methanol/99% dichloromethane) to give the title compound, containing 0.20 mol of water; mp 138°-139° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05273977
출처 데이터셋uspto-grants-1993_12
ORD IDord-991b6fd6abbe4575995966e5a11eeeec
출처 메모uspto-grants-1993_12