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HRID 1877454생성일: 2026년 10월 27일

Dichloromethane → 5-(9H-carbazol-4-yl)pyridine-2-carbonitrile

https://huagongshe.com/reaction/1877454

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Cesium carbonateHCID 10796—
반응물2-Cyanopyridine-5-boronic acid pinacol esterHCID 16414188—
반응물4-TrifluoromethanesulphonyloxycarbazoleHCID 58338323—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물5-(9H-carbazol-4-yl)pyridine-2-carbonitrileHCID 5833817435.1%

반응 단계

0.72 g of 2-cyano-5-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)pyridine, 3.3 g of caesium carbonate and 92 mg of 1,1′-bis(diphenyl-phosphino)ferrocenepalladium(II) dichloride as a complex with dichloromethane (1/1) [PdCl2(dppf).CH2Cl2] are successively added, under argon, to a solution of 0.8 g of 4-trifluoromethanesulphonyloxycarbazole, obtained in stage 1 of Example 1, in a mixture of 37 ml of dioxane and 12 ml of water. The reaction mixture is refluxed for 4 hours, cooled to ambient temperature, filtered through celite and concentrated under reduced pressure. The residue is subsequently purified by silica gel chromatography, elution being carried out with a mixture of cyclohexane and ethyl acetate (85/15 by volume), so as to give 0.24 g of 5-(9H-carbazol-4-yl)pyridine-2-carbonitrile in the form of a yellow solid, the characteristics of which are the following:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08309721B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-706ae1abb02f4764b4715e4440b369f7
출처 메모uspto-grants-2012_11