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HRID 1617174作成日:2026年10月25日

(2S)-2-aminopentan-1-ol → (S)-2-(4-((2-Amino-4-(1-hydroxypentan-2-ylamino)-6-methylpyrimidin-5-yl)methyl)-3-methoxyphenyl)acetonitrile

https://huagongshe.com/reaction/1617174

反応式

関与物質

役割名称HCID仕込み量
反応物(2S)-2-aminopentan-1-olHCID 6951248—
反応物2-(4-((2-Amino-4-chloro-6-methylpyrimidin-5-yl)methyl)-3-methoxyphenyl)acetonitrileHCID 86633402—
溶媒Ethyl AcetateHCID 8857—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物(S)-2-(4-((2-Amino-4-(1-hydroxypentan-2-ylamino)-6-methylpyrimidin-5-yl)methyl)-3-methoxyphenyl)acetonitrileHCID 68955240—

反応条件

温度140 °C

反応手順

(S)-2-Aminopentan-1-ol (0.136 g) was added to a solution of the product from step (iii) in NMP (2 mL). The resulting mixture was stirred at 140° C. for 50 h then diluted with EtOAc and washed with saturated NaHCO3 solution and saturated brine. The organic phase was dried, filtered and evaporated. The crude product was purified by column chromatography, elution gradient 5 to 10% MeOH in DCM to give the subtitle compound, 0.095 g.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08765939B2
出典データセットuspto-grants-2014_07
ORD IDord-6913b3a48b284ac8ad14246b53620be3
出典メモuspto-grants-2014_07