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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 404138생성일: 2026년 10월 24일

2-Aminopyridine → 2-Pyridyl-2-quinolylamine

https://huagongshe.com/ko/reaction/404138

반응식

참여 물질

역할이름HCID투입량
반응물2-AminopyridineHCID 10439—
반응물2-BromoquinolineHCID 2762756—
반응물HCID 178418922HCID 178418922—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
생성물2-Pyridyl-2-quinolylamineHCID 534011245%

반응 단계

2-Bromoquinoline, I (500 mg, 2.40 mmol), 2-aminopyridine (249 mg, 2.64 mmol), tBuOK (404 mg, 3.60 mmol), (±)-BINAP (6 mg, 0.01 mmol) and Pd2(dba)3 (5.5 mg, 0.006 mmol) were stirred in toluene (10 mL) at 90° C. under Ar(g) for 21 h. The reaction mixture was then diluted with CH2Cl2 (10 mL) and silica was added, followed by the removal of the solvent under reduced pressure. The resulting dry load material was purified by silica gel column chromatography eluting with CH2Cl2/MeOH (100:1 then 100:2) to furnish II as a colourless oil (344 mg, 45%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08748458B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-b01f6dbe9a5740c582c3a8b9464be9af
출처 메모uspto-grants-2014_06