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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 547914생성일: 2026년 10월 27일

5-Bromopyrimidine → 4-(Pyrimidin-5-ylamino)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/547914

반응식

참여 물질

역할이름HCID투입량
반응물5-BromopyrimidineHCID 78344—
반응물4-Amino-1-Boc-piperidineHCID 1268291—
반응물HCID 178418922HCID 178418922—
촉매Binap, (A+-)-HCID 634876—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
생성물4-(Pyrimidin-5-ylamino)-piperidine-1-carboxylic acid tert-butyl esterHCID 6719821147%

반응 단계

A mixture of 5-bromo-pyrimidine (1.59 g, 10.00 mmol, 1.0 equiv; commercially available), 4-amino-piperidine-1-carboxylic acid tert-butyl ester (2.00 g, 10.00 mmol, 1.0 equiv), rac-2,2′-bis(diphenylphosphino)-1,1′-binaphthalene (0.25 g, 0.40 mmol, 0.04 equiv), tris(dibenzylideneacetone)dipalladium(0) (0.21 g, 0.20 mmol, 0.02 equiv) and KOtert-Bu (1.35 g, 12.01 mmol, 1.2 equiv) in toluene (10 mL) was heated under Ar by microwave irradiation to 100° C. for 2 h. The crude reaction mixture was filtered through Hyflo Super Cel, a sat. solution of sodium chloride (100 mL) was added and the mixture extracted with ethyl acetate (3×50 mL). The combined organic phases were concentrated by evaporation under reduced pressure and the residue purified by silica column chromatography using a MPLC system (CombiFlash Companion, Isco Inc.) eluting with a gradient of heptane (+1% triethylamine)/ethyl acetate to provide 1.30 g (47%) of the title compound. MS (ISP): 279.1 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07939661B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-3f32390041ba44ada63f8874ed90e3fd
출처 메모uspto-grants-2011_05