돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20074생성일: 2026년 10월 23일

4-Bromopyridine → Ethyl 4-(pyridin-4-ylamino)piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/20074

반응식

참여 물질

역할이름HCID투입량
반응물4-BromopyridineHCID 14268—
반응물Ethyl 4-amino-1-piperidinecarboxylateHCID 100867—
반응물Binap, (A+-)-HCID 634876—
반응물Sodium t-butoxideHCID 23676156—
촉매palladium(II) acetateHCID 167845—
용매TolueneHCID 1140—
생성물Ethyl 4-(pyridin-4-ylamino)piperidine-1-carboxylateHCID 2229322341.1%

반응 단계

A solution of ethyl 4-aminopiperidine-1-carboxylate (2.20 g, 12.7 mmol), 4-bromopyridine (3.47 g, 17.8 mmol), sodium t-butoxide (4.54 g, 47.2 mmol), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.398 g, 0.639 mmol) and palladium acetate (0.143 g, 0.639 mmol) in toluene (40 mL) was heated at 60° C. overnight. The reaction was cooled and partitioned between ethyl acetate and water. The aqueous layer was washed 3 times with methylene chloride, and the combined organic layers dried over sodium sulfate. The crude product was purified by chromatography (silica gel, 0 to 10% {5% ammonium hydroxide in methanol}in methylene chloride gradient elution), which gave the title compound (1.3 g, 41% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745427B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-101a650b45d542b081d56e34c403fdfc
출처 메모uspto-grants-2010_06