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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 128957생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/128957

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 20) (0.83 g , 2.7 mmon) 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 번호US05466698
출처 데이터셋uspto-grants-1995_11
ORD IDord-c63b4b7cd220418291a8b91ca4b86a51
출처 메모uspto-grants-1995_11