[C:1]([NH:4][C:5]1[S:6][C:7]([S:10][CH2:11][C:12]([OH:14])=O)=[CH:8][N:9]=1)(=[O:3])[CH3:2].C1C=CC2N(O)N=NC=2C=1.Cl.C(N=C=NCCCN(C)C)C.Cl.[NH2:38][CH2:39][C:40](=[O:43])[CH2:41][CH3:42].C(N(CC)CC)C>CN(C=O)C.O>[C:1]([NH:4][C:5]1[S:6][C:7]([S:10][CH2:11][C:12]([NH:38][CH2:39][C:40](=[O:43])[CH2:41][CH3:42])=[O:14])=[CH:8][N:9]=1)(=[O:3])[CH3:2]A mixture of [[2-(acetylamino)-5-thiazolyl]thio]acetic acid (9.0 g, 38.8 mmol), HOBT (5.94 g, 38.8 mmol) and ethyldimethylaminopropylcarbodiimide hydrochloride salt (11.16 g, 58.2 mmol) in DMF (50 mL) was stirred at 0° C. for 0.5 h. To this mixture was added 1-amino-2-butanone hydrochloride (5.27 g, 42.7 mmol) followed by triethylamine (15 mL, 107.5 mmol). The mixture was stirred at 0° C. for 0.5 h and at rt for 1 h. Water (200 mL) was added to the mixture and the product was extracted with methylene chloride containing 10% MeOH (5×100 mL). The methylene chloride extract was dried over Na2SO4 and concentrated. The residue was triturated with water and the precipitated solid product was collected by filtration. It was dried to obtain the desired product (10.5 g, 90%), mp 195-196° C.
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