돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 609732생성일: 2026년 10월 24일

5-bromo-3-[2-(N,N-dimethylamino)ethyl]-1-benzoylindole → 5-(3,4-dihydropyran-4-yl)-3-[2-(N,N-dimethylamino)ethyl]-1-benzoylindole

https://huagongshe.com/ko/reaction/609732

반응식

참여 물질

역할이름HCID투입량
반응물5-bromo-3-[2-(N,N-dimethylamino)ethyl]-1-benzoylindoleHCID 19600443—
반응물4-Tributylstannyl-3,4-dihydropyranHCID 19600452—
용매TolueneHCID 1140—
생성물5-(3,4-dihydropyran-4-yl)-3-[2-(N,N-dimethylamino)ethyl]-1-benzoylindoleHCID 1960044817%

반응 단계

A solution of 5-bromo-3-[2-(N,N-dimethylamino)ethyl]-1-benzoylindole (Example 5a, 180 mg 0.48 mmol), 4-tributylstannyl-3,4-dihydropyran (180 mg, 0.48 mmol) and tetrakistriphenyphosphine palladium (118 mg, 0.1 mmol) in toluene (3 mL) was stirred at 100-110° C. A second portion of catalyst was added after 1 h and heating was continued overnight. After removal of the solvent in vacuo, flash chromatography on silica gel (2-6% 2M methanolic ammonia in dichloromethane) yielded 5-(3,4-dihydropyran-4-yl)-3-[2-(N,N-dimethylamino)ethyl]-1-benzoylindole (30.5 mg, 17%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05998438
출처 데이터셋uspto-grants-1999_12
ORD IDord-1f04ef2904a540abb5f21fe0815090e6
출처 메모uspto-grants-1999_12