CC([N:5]([C:9]1([C:12]([NH:14][N:15]2[CH:19]=[CH:18][CH:17]=[CH:16]2)=[O:13])[CH2:11][CH2:10]1)C(=O)[O-])(C)C.[ClH:20].CCOC(C)=O.CCCCCC.II>C(OCC)(=O)C.C(O)(C)C>[ClH:20].[NH2:5][C:9]1([C:12]([NH:14][N:15]2[CH:19]=[CH:18][CH:17]=[CH:16]2)=[O:13])[CH2:11][CH2:10]1
To a stirred solution consisting of 1,1-dimethylethyl-[1-[(1H-pyrrol-1-ylamino)carbonyl]cyclopropyl]carbamate (3.18 g) in ethyl acetate/isopropanol (70 ml) was added excess ethereal HCl. After stirring for 48 hours at room temperature, the reaction appeared complete by thin layer chromatography (TLC) (silica gel, 30% EtOAc/hexane, I2 stain). The solid product was filtered under nitrogen and recrystallized from ether/ethanol to afford 1.20 g of the product as a solid, m.p. 238°-240° C.
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