CS(O)(=O)=O.C(OC([N:13]1[CH2:20][CH2:19][CH2:18][C@@:14]1([CH3:21])[C:15]([OH:17])=[O:16])=O)(C)(C)C.C(N(CC)CC)C>ClCCCl>[CH3:21][C@@:14]1([C:15]([OH:17])=[O:16])[CH2:18][CH2:19][CH2:20][NH:13]1Methanesulfonic acid (252 mg, 2.6 mmol) was added to a solution of (S)—N-(tert-butoxycarbonyl)-2-methylproline (500 mg, 2.2 mmol) and 1,2-dichloroethane (2.53 g), and the mixture was stirred at 25° C. for 3 hours. When triethylamine (265 mg, 2.6 mmol) was added thereto, a solid was precipitated. The solid was sufficiently precipitated, and then the solution was stirred at 25° C. for 30 minutes and further stirred at 25° C. for 2 hours. Thereafter, the solid was then separated by filtration under reduced pressure. The solid was washed with 1,2-dichloroethane (0.2 mL), and then was subjected to vacuum drying. Thereby, the titled compound was produced as a white solid (197 mg, yield of 69%).
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