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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1829048생성일: 2026년 10월 26일

Triethylamine → 3-[5-(3-dimethylamino-prop-1-ynyl)-3H-isobenzofuran-1-ylidene]-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/1829048

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물N,N-DimethylpropargylamineHCID 81643—
반응물3-(5-Bromo-2-benzofuran-1(3H)-ylidene)-1,3-dihydro-2H-indol-2-oneHCID 69659242—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418397HCID 178418397—
용매MethanolHCID 887—
용매DimethylformamideHCID 6228—
생성물3-[5-(3-dimethylamino-prop-1-ynyl)-3H-isobenzofuran-1-ylidene]-1,3-dihydro-indol-2-oneHCID 6965915168.2%

반응 조건

온도65 °C

반응 단계

To a mixture of 3-(5-bromo-3H-isobenzofuran-1-ylidene)-1,3-dihydro-indol-2-one (467 mg, 1.42 mmol), 1-dimethylamino-2-propyne (473 mg, 5.69 mmol), copper(I) iodide (48 mg, 0.25 mmol), triethylamine (287 mg, 2.84 mmol) in DMF (5 ml), was added tetrakis(triphenylphosphine)palladium (100 mg, 0.086 mmol). The mixture was heated at 65° C. under argon for 16 hours, and then cooled to room temperature. The mixture was diluted with MeOH (100 ml). The insoluble material was removed by filtration, and the filtrate solution was concentrated and then diluted with EtOAc (200 ml). The resulting mixture was washed with brine (3×100 ml), dried over anhydrous Na2SO4, and concentrated to give a dark-brown residue. Purification of the residue by silica gel column chromatography, eluted with a gradient of MeOH in CHCl3, afforded 3-[5-(3-dimethylamino-prop-1-ynyl)-3H-isobenzofuran-1-ylidene]-1,3-dihydro-indol-2-one as a brown solid (320 mg, 68%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07060844B2
출처 데이터셋uspto-grants-2006_06
ORD IDord-be0939c8a573433199b87c0311c98046
출처 메모uspto-grants-2006_06