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HRID 1046529作成日:2026年10月26日

Ethyl 4-aminocyclohexanecarboxylate → 4-{4-[8-(1-Hydroxy-1-methyl-ethyl)-imidazo[1,2-a]pyridin-3-yl]-pyrimidin-2-ylamino}-cyclohexanecarboxylic acid ethyl ester

https://huagongshe.com/reaction/1046529

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 4-aminocyclohexanecarboxylateHCID 409963—
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4-{4-[8-(1-Hydroxy-1-methyl-ethyl)-imidazo[1,2-a]pyridin-3-yl]-pyrimidin-2-ylamino}-cyclohexanecarboxylic acid ethyl esterHCID 6661621184.5%

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 (0.19 g), 4-amino-cyclohexanecarboxylic acid ethyl ester (0.31 g) in NMP (2 mL) was stirred at 100° C. for 3 h. The reaction mixture was cooled to RT, and diluted with water. The resulting solid was filtered and dried, then purified by ISCO using 100% DCM to 10% MeOH/DCM. Fractions were collected, concentrated, and titurated with EtOAc/hexane. The resulting solid was filtered and dried at 50° C. under vacuum overnight to provide 4-{4-[8-(1-hydroxy-1-methyl-ethyl)-imidazo[1,2-a]pyridin-3-yl]-pyrimidin-2-ylamino}-cyclohexanecarboxylic acid ethyl ester (0.215 g).

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-1dd7c7df0772475aa911071df8d9509b
出典メモuspto-grants-2013_10