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HRID 128953作成日:2026年10月26日

Acetyl chloride → N-[6-[4-(3,6-Dihydro-4-phenyl-1(2H)-pyridinyl)-1-butynyl]-3-pyridinyl]acetamide

https://huagongshe.com/reaction/128953

反応式

関与物質

役割名称HCID仕込み量
反応物Acetyl chlorideHCID 6367—
反応物TriethylamineHCID 8471—
反応物6-[4-(3,6-Dihydro-4-phenyl-1(2H)-pyridinyl)-1-butynyl]-3-pyridinamineHCID 10086348—
溶媒DichloromethaneHCID 6344—
生成物N-[6-[4-(3,6-Dihydro-4-phenyl-1(2H)-pyridinyl)-1-butynyl]-3-pyridinyl]acetamideHCID 19960121—

反応手順

A solution of 6-[4-(3,6-dihydro-4-phenyl-1(2H)-pyridinyl)-1-butynyl]-3-pyridinamine (Example 20) (1.5 g, 0.005 mol), triethylamine (0.76 mL, 0.0054 mol) and N,N-dimethylaminopyridine (catalytic amount) in 50 mL of dichloromethane is cooled to 0° C. and acetyl chloride (0.42 mL, 0.006 mol) is added dropwise. The cold bath is removed and the solution is stirred at room temperature for 1 hour. The reaction is quenched with saturated aqueous sodium bicarbonate, the organic layer is washed with water and dried (sodium sulfate), and the solvent is removed under reduced pressure. The residue is chromatographed (silica gel, 2% methanol/98% dichloromethane) to give the title compound, containing 0.35 mol of water; mp 158.5°-159.5° 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-60286149b27246d9a67dad7ff08b63f8
出典メモuspto-grants-1995_11