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HRID 1186464作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Methylthio)-4-(tributylstannyl)pyrimidineHCID 2763261—
反応物(3-Bromo-imidazo[1,2-a]pyrazin-8-yl)-methyl-carbamic acid tert-butyl esterHCID 58818944—
触媒Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
溶媒TolueneHCID 1140—
生成物Methyl-[3-(2-methylsulfanyl-pyrimidin-4-yl)-imidazo[1,2-a]pyrazin-8-yl]-carbamic acid tert-butyl esterHCID 68226929—

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08673905B2
出典データセットuspto-grants-2014_03
ORD IDord-21a62a00dcdf4f3c84dfd6684f068520
出典メモuspto-grants-2014_03