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HRID 1046528作成日:2026年10月27日

4-(Methanesulfonylmethyl)cyclohexan-1-amine → 2-{3-[2-(4-Methanesulfonylmethyl-cyclohexylamino)-pyrimidin-4-yl]-imidazo[1,2-a]pyridin-8-yl}-propan-2-ol

https://huagongshe.com/reaction/1046528

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Methanesulfonylmethyl)cyclohexan-1-amineHCID 58345904—
反応物2-[3-(2-Methylsulfinyl-pyrimidin-4-yl)-imidazo[1,2-a]pyridin-8-yl]-propan-2-olHCID 66616285—
溶媒WaterHCID 962—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物2-{3-[2-(4-Methanesulfonylmethyl-cyclohexylamino)-pyrimidin-4-yl]-imidazo[1,2-a]pyridin-8-yl}-propan-2-olHCID 5855316952.8%

反応条件

温度100 °C

反応手順

A mixture of 2-[3-(2-methylsulfinyl-pyrimidin-4-yl)-imidazo[1,2-a]pyridin-8-yl]-propan-2-ol (75 mg), 4-methanesulfonylmethyl-cyclohexylamine (162 mg), and TEA (0.165 mL) in NMP (2 mL) was stirred at 100° C. overnight. The reaction mixture was then cooled to RT, and diluted with water. The resulting precipitate was filtered and dried, then purified by ISCO using 100% DCM to 10% MeOH/DCM. The fractions were collected, concentrated, and titurated with EtOAc. The resulting solid was filtered and dried at 50° C. under vacuum overnight to provide 2-{3-[2-(4-methanesulfonylmethyl-cyclohexylamino)-pyrimidin-4-yl]-imidazo[1,2-a]pyridin-8-yl}-propan-2-ol (Compound 1, 55.5 mg). Mp=223-224° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08569306B2
出典データセットuspto-grants-2013_10
ORD IDord-8172da2e90f4453281532ffa792a72a2
出典メモuspto-grants-2013_10