C[O:2][C:3]([C:5]1([NH2:11])[CH2:10][CH2:9][CH2:8][CH2:7][CH2:6]1)=[O:4].[C:12](OC(OC(C)(C)C)=O)(OC(C)(C)C)=[O:13].C(N(CC)CC)C.[S:34]1[CH2:38][CH2:37][NH:36][CH2:35]1>C(Cl)Cl>[S:34]1[CH2:38][CH2:37][N:36]([C:12]([NH:11][C:5]2([C:3]([OH:2])=[O:4])[CH2:10][CH2:9][CH2:8][CH2:7][CH2:6]2)=[O:13])[CH2:35]1A solution of 78 mg (0.6 mmol) of N,N-dimethylaminopyridine and 1 g (6.36 mmol) of 1-aminocyclohexanecarboxylic acid methyl ester in methylene chloride was added to a solution of 1.39 mg (6.36 mmol) of di-t-butyl dicarbonate in 10 ml of methylene chloride, and the mixture was stirred at room temperature for 30 minutes. Thereafter, a solution of 1.29 g (12.7 mmol) of triethylamine and 680 mg (7.6 mmol) of thiazolidine in methylene chloride was added thereto, and the mixture was stirred at room temperature overnight. After the reaction solution was concentrated, the residue was dissolved in ethyl acetate, and the mixture was washed with water, a 10% aqueous potassium hydrogensulfate solution, a saturated aqueous sodium hydrogencarbonate solution and then saturated brine, followed by drying with anhydrous sodium sulfate. After the solvent was distilled off under reduced pressure, tetrahydrofuran and 1N aqueous sodium hydroxide solution were added to the residue, and the mixture was heated under reflux for 3 hours. After ether was added to the reaction solution to wash it, the aqueous layer was neutralized by concentrated hydrochloric acid, and it was extracted with ethyl acetate. After the obtained organic layer was washed with saturated brine, it was dried with anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain 1.1 g (66%) of the title compound.
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