反应详情

24 mg of (1S,2S)-2-(4-biphenylyl)-3-(3,4-dichlorophenyl)-1-methylpropylamine obtained in Example 115, 14 mg of monoethyl adipate and 10 mg of 4-dimethylaminopyridine were dissolved in 2 ml of methylene chloride, and 15 mg of 1-ethyl-3-(3-dimethyaminopropyl)carbodiimide hydrochloride was added thereto with stirring under cooling with ice. The mixture was stirred at room temperature for 3 hours. The reaction solution was diluted with ethyl ether, then sequentially washed with a 10% citric acid aqueous solution, a saturated sodium hydrogencarbonate aqueous solution and a saturated sodium chloride aqueous solution, and dried over anhydrous magnesium sulfate. Then, the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (Wakogel™ C-200, 1 g, hexane/ethyl acetate=2/1), and 28 mg of the obtained amide compound was dissolved in 1 ml of methanol. Then, 0.5 ml of a 2N sodium hydroxide aqueous solution was added thereto, and the mixture was stirred at room temperature overnight. The reaction solution was acidified with 1N hydrochloric acid and then subjected to liquid separation by an addition of ethyl ether and water. The organic layer was collected by separation, then washed with a saturated sodium chloride aqueous solution and dried over anhydrous magnesium sulfate. The drying agent was separated by filtration, and then the solvent was distilled off. The residue was treated with a liquid mixture of isopropyl ether and ethyl ether to obtain 16 mg (yield: 49%) of the above-identified compound as white crystalline powder having a melting point of from 123° to 124° C. and

1. temperatureunder cooling with ice
2. stirringThe mixture was stirred at room temperature for 3 hours
3. washsequentially washed with a 10% citric acid aqueous solution
4. dry with materiala saturated sodium hydrogencarbonate aqueous solution and a saturated sodium chloride aqueous solution, and dried over anhydrous magnesium sulfate
5. distillationThen, the solvent was distilled off under reduced pressure
6. customThe residue was purified by silica gel column chromatography (Wakogel™ C-200, 1 g, hexane/ethyl acetate=2/1), and 28 mg of the obtained amide compound
7. dissolutionwas dissolved in 1 ml of methanol
8. additionThen, 0.5 ml of a 2N sodium hydroxide aqueous solution was added
9. stirringthe mixture was stirred at room temperature overnight
10. customsubjected to liquid separation by an addition of ethyl ether and water
11. customThe organic layer was collected by separation
12. washwashed with a saturated sodium chloride aqueous solution
13. dry with materialdried over anhydrous magnesium sulfate
14. customThe drying agent was separated by filtration
15. distillationthe solvent was distilled off
16. additionThe residue was treated with a liquid mixture of isopropyl ether and ethyl ether