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HRID 968523作成日:2026年10月27日

Dicyclohexylcarbodiimide → (3R)-4-(4-toluenesulfonyl)thiomorpholine-3-carboxylic acid [3-(pyridin-3-yl)]-propyl ester

https://huagongshe.com/reaction/968523

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclohexylcarbodiimideHCID 10868—
反応物3-PyridinepropanolHCID 17861—
反応物(3R)-4-(4-toluenesulfonyl)thiomorpholine-3-carboxylic acidHCID 69415969—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物(3R)-4-(4-toluenesulfonyl)thiomorpholine-3-carboxylic acid [3-(pyridin-3-yl)]-propyl esterHCID 8659859992.7%

反応手順

0.301 g (1 mmol) of (3R)-4-(4-toluenesulfonyl)thiomorpholine-3-carboxylic acid, 0.206 g (1.5 mmol) of 3-(pyridin-3-yl)-propanol, 0.088 g (0.33 mmol) of CAS, 0.227 g (1.2 mmol) of DCC and 0.04 g (0.33 mmol) of DMAP were dissolved in 15 mL of CH2Cl2. The mixture was stirred for 24 h at room temperature. The solid was filtrated and the solvent was evaporated. The residual was dissolved in a suitable amount of ethyl acetate (20 ml) and then the mixture was filtered to remove insoluble substance. The ethyl acetate was added to 60 ml and then the liquid was washed with 10% NaHCO3 solution, saturated NaCl solution and dried over Na2SO4. After the drying agent was removed and part of ethyl acetate was evaporated, the crude product was purified by flash column chromatography (eluent: ethyl acetate:cyclohexane=1:1) to obtain the product as a oil (0.39 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07304057B2
出典データセットuspto-grants-2007_12
ORD IDord-f031494d917641188ad9f9b37003c470
出典メモuspto-grants-2007_12