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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1186464생성일: 2026년 10월 26일

2-(Methylthio)-4-(tributylstannyl)pyrimidine → Methyl-[3-(2-methylsulfanyl-pyrimidin-4-yl)-imidazo[1,2-a]pyrazin-8-yl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1186464

반응식

참여 물질

역할이름HCID투입량
반응물2-(Methylthio)-4-(tributylstannyl)pyrimidineHCID 2763261—
반응물(3-Bromo-imidazo[1,2-a]pyrazin-8-yl)-methyl-carbamic acid tert-butyl esterHCID 58818944—
촉매Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
용매TolueneHCID 1140—
생성물Methyl-[3-(2-methylsulfanyl-pyrimidin-4-yl)-imidazo[1,2-a]pyrazin-8-yl]-carbamic acid tert-butyl esterHCID 68226929—

반응 단계

2-Methylsulfanyl-4-tributylstannanyl-pyrimidine (19.1 g, 46.0 mmol) was stirred in degassed toluene (achieved by bubbling nitrogen though solvent for 2 hours) (200 mL) under nitrogen, then (3-bromo-imidazo[1,2-a]pyrazin-8-yl)-methyl-carbamic acid tert-butyl ester (13.1 g, 40.0 mmol) (from Example 7 supra) was added followed by bis(triphenylphosphine)palladium (II) chloride (1.12 g, 1.60 mmol) and the reaction was heated at reflux. The reaction was cooled to room temperature and concentrated to dryness. The residue was purified by column chromatography on silica gel (petroleum ether to EtOAc, TLC Rf=0.17, 20% EtOAc in petroleum ether) and then triturated with DIPE to give methyl-[3-(2-methylsulfanyl-pyrimidin-4-yl)-imidazo[1,2-a]pyrazin-8-yl]-carbamic acid tert-butyl ester. (Yield 8.00 g, 54%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08673905B2
출처 데이터셋uspto-grants-2014_03
ORD IDord-21a62a00dcdf4f3c84dfd6684f068520
출처 메모uspto-grants-2014_03