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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72786생성일: 2026년 10월 23일

Triphenylarsine → (2S)-N2-[2-chloro-5-(3,3-diethoxyprop-1-ynyl)pyrimidin-4-yl]-4-methyl-pentane-1,2-diamine

https://huagongshe.com/ko/reaction/72786

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylarsineHCID 11773—
반응물3,3-DiethoxypropyneHCID 66285—
반응물tert-butyl N-[(2S)-2-[(5-bromo-2-chloro-pyrimidin-4-yl)amino]-4-methyl-pentyl]carbamateHCID 86695597—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
용매TriethylamineHCID 8471—
생성물(2S)-N2-[2-chloro-5-(3,3-diethoxyprop-1-ynyl)pyrimidin-4-yl]-4-methyl-pentane-1,2-diamineHCID 86695596—

반응 단계

To a solution of tert-butyl N-[(2S)-2-[(5-bromo-2-chloro-pyrimidin-4-yl)amino]-4-methyl-pentyl]carbamate 5.0 g (12.3 mmole) in toluene (36 mL) and triethyl amine (7.2 mL) was added under nitrogen, 3,3-diethoxyprop-1-yne 2.8 mL (19.7 mmole), Pd2(dba)3 1.1 g (1.23 mmole), and triphenylarsine 3.8 g (12.3 mmole). The contents were heated to 70 degrees for 24 hrs. After cooling to room temperature, the reaction mixture was filtered through CELITE™ and then concentrated under vacuum. The crude product was columned over silica gel using hexane/ethyl acetate (0-30%) to afford (2S)—N2-[2-chloro-5-(3,3-diethoxyprop-1-ynyl)pyrimidin-4-yl]-4-methyl-pentane-1,2-diamine. LCMS (ESI) 455 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829012B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-59c3c39d263c4e4c975b19f4d07361a6
출처 메모uspto-grants-2014_09