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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 251022생성일: 2026년 10월 26일

Indole → 3-Indol-1-yl-pyridine-2-carbonitrile

https://huagongshe.com/reaction/251022

반응식

참여 물질

역할이름HCID투입량
반응물IndoleHCID 798—
반응물Cesium carbonateHCID 10796—
반응물3-Bromopyridine-2-carbonitrileHCID 817694—
촉매1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
생성물3-Indol-1-yl-pyridine-2-carbonitrileHCID 6727170689%

반응 조건

온도110 °C

반응 단계

To a solution of 3-bromo-2-cyanopyridine (Sakamoto, T. et al., Chem. Pharm. Bull. 1985, 33(2), 565-571) (340 mg, 1.86 mmol) and indole (436 mg, 3.72 mmol) in toluene (15 mL) was added Cs2CO3 (737 mg, 2.26 mmol), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (83 mg, 0.143 mmol) and Pd2(dba)3 (42 mg, 0.046 mmol) and the reaction stirred at 110° C. for 2.5 d. The mixture was concentrated and purified by column chromatography on silica gel (EtOAc/Hexanes, 2:1) to give 3-indol-1-yl-pyridine-2-carbonitrile (362 mg, 89%) as a beige solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863293B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-c75c30a8e3a5439193376c99a7645a8a
출처 메모uspto-grants-2011_01