돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1069677생성일: 2026년 10월 23일

3,5-Dimethyl-1-hexyn-3-ol → rac-(Z)-1,3-dihydro-4-(3,5-dimethyl-3-hydroxy-1-hexynyl)-3-[(3-methoxy-1H-pyrrol-2-yl)methylene]-2H-indol-2-one

https://huagongshe.com/ko/reaction/1069677

반응식

참여 물질

역할이름HCID투입량
반응물3,5-Dimethyl-1-hexyn-3-olHCID 61018—
반응물(Z)-1,3-dihydro-4-iodo-3-[(3-methoxy-1H-pyrrol-2-yl)methylene]-2H-indol-2-oneHCID 15548053—
촉매HCID 178418476HCID 178418476—
용매DimethylformamideHCID 6228—
용매TriethylamineHCID 8471—
생성물rac-(Z)-1,3-dihydro-4-(3,5-dimethyl-3-hydroxy-1-hexynyl)-3-[(3-methoxy-1H-pyrrol-2-yl)methylene]-2H-indol-2-oneHCID 9841998—

반응 단계

Using Method C above, 3,5-dimethyl-1-hexyn-3-ol (61 mg, 0.48 mmol) (Aldrich) was coupled with (Z)-1,3-dihydro-4-iodo-3-[(3-methoxy-1H-pyrrol-2-yl)methylene]-2H-indol-2-one (Starting Material 2 supra) (146 mg, 0.4 mmol) using (Ph3P)2PdCl2 (20 mg) and Cul (10 mg) as catalyst in DMF (2 mL) and Et3N (2 mL) as solvent at 70° C. for 15 h to yield rac-(Z)-1,3-dihydro-4-(3,5-dimethyl-3-hydroxy-1-hexynyl)-3-[(3-methoxy-1H-pyrrol-2-yl)methylene]-2H-indol-2-one. (Yield 87 mg, 60%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06252086B1
출처 데이터셋uspto-grants-2001_06
ORD IDord-305e10590a264bccbe5980c4b0cd506f
출처 메모uspto-grants-2001_06