돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53646생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/53646

반응식

참여 물질

역할이름HCID투입량
반응물Acetyl chlorideHCID 6367—
반응물TriethylamineHCID 8471—
반응물6-[4-(3,6-Dihydro-4-phenyl-1(2H)-pyridinyl)-1-butynyl]-3-pyridinamineHCID 10086348—
용매DichloromethaneHCID 6344—
생성물N-[6-[4-(3,6-Dihydro-4-phenyl-1(2H)-pyridinyl)-1-butynyl]-3-pyridinyl]acetamideHCID 19960121—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05620988
출처 데이터셋uspto-grants-1997_04
ORD IDord-17315cbe92514012a722ec0dd6c909d4
출처 메모uspto-grants-1997_04