反应 #50254

反应方程式

N-[dimethylaminopropyl]-N'-ethylcarbodiimide hydrochloride

trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxylic acid

1-hydroxybenzotriazole

4-methylmorpholine

L-hydroxyproline ethyl ester hydrochloride

→

N-[[trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecan-10-yl]-carbonyl]-trans 4-hydroxy-L-proline ethyl ester

溶剂

methylene chloride

methylene chloride

反应条件

后处理

1. 1
   温度to warm up to room temperature
2. 2
   洗涤the organic layer is washed with 1N hydrochloric acid, saturated sodium bicarbonate
3. 3
   干燥dried (MgSO4)
4. 4
   其他the solvent is evaporated
5. 5
   其他The product is purified by silica gel chromatography (80% ethyl acetate/hexane)

实验过程

The enantiomer of trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxylic acid of Example 16 (0.23 g, 0.80 mmol), 1-hydroxybenzotriazole (0.11 g, 0.80 mmol), 4-methylmorpholine (0.22 mL, 2.0 mmol), and L-hydroxyproline ethyl ester hydrochloride (0.16 g, 0.80 mmol) are dissolved in methylene chloride (5.0 mL), and the reaction is cooled to 0° C. To this solution is added N-[dimethylaminopropyl]-N'-ethylcarbodiimide hydrochloride (0.31 g, 1.60 mmol), and the reaction is allowed to warm up to room temperature and stirred overnight. The reaction is diluted with more methylene chloride, and the organic layer is washed with 1N hydrochloric acid, saturated sodium bicarbonate, dried (MgSO4), and the solvent is evaporated. The product is purified by silica gel chromatography (80% ethyl acetate/hexane) to give N-[[trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecan-10-yl]-carbonyl]-trans 4-hydroxy-L-proline ethyl ester as a single enantiomer, [α]D +5.73° (c=4.1 mg/ml,CH2Cl2) which is assigned the 3R, 10S configuration.

来源