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HRID 128957作成日:2026年10月26日

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

https://huagongshe.com/reaction/128957

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物PropanalHCID 527—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物6-[4-(3,6-Dihydro-4-phenyl-1(2H)-pyridinyl)-1-butynyl]-3-pyridinamineHCID 10086348—
溶媒1,1-DichloroethaneHCID 6365—
生成物6-[4-(3,6-Dihydro-4-phenyl-1(2H)-pyridinyl)-1-butynyl]-N-propyl-3-pyridinamineHCID 19960149—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05466698
出典データセットuspto-grants-1995_11
ORD IDord-c63b4b7cd220418291a8b91ca4b86a51
出典メモuspto-grants-1995_11