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HRID 1989017作成日:2026年10月27日

4-Chloro-2-(methylthio)pyrimidine-5-carboxylic acid ethyl ester → 4-[Cyclohexyl-(2-ethoxycarbonyl-ethyl)-amino]-2-methylsulfanyl-pyrimidine-5-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1989017

反応式

関与物質

役割名称HCID仕込み量
反応物4-Chloro-2-(methylthio)pyrimidine-5-carboxylic acid ethyl esterHCID 80008—
反応物DiisopropylethylamineHCID 81531—
反応物Ethyl 3-(cyclohexylamino)propanoateHCID 243063—
溶媒DichloromethaneHCID 6344—
生成物4-[Cyclohexyl-(2-ethoxycarbonyl-ethyl)-amino]-2-methylsulfanyl-pyrimidine-5-carboxylic acid ethyl esterHCID 6858349684%

反応手順

3-Cyclohexylamino-propionic acid ethyl ester (1.0 g, 5.0 mmol) and 4-chloro-2-methylsulfanyl-pyrimidine-5-carboxylic acid ethyl ester (1.17 g, 5.02 mmol) were combined in DCM (15 mL) and diisopropylethylamine (0.81 g, 6.3 mmol) was added. After 16 h, the solution was partitioned between water and DCM and the organic layer was dried (MgSO4) and concentrated. Chromatography (0-20% EtOAc/hexanes gradient) provided 1.63 g (84%) of the title compound. 1H-NMR (400 MHz, CDCl3) δ ppm 8.39 (s, 1H) 5.30 (s, 1H), 4.30 (q, 2H, J=7.1 Hz), 4.14 (q, 1H, J=7.1 Hz), 3.76-3.80 (m, 2H), 2.65-2.69 (m, 2H), 2.49 (s, 3H), 1.81-1.84 (m, 2H), 1.34-1.40 (m, 7H), 1.12-1.27 (m, 7H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07642270B2
出典データセットuspto-grants-2010_01
ORD IDord-885d4f060d6e4008ad5740447204df58
出典メモuspto-grants-2010_01