反应 #8265

ord-23028e4a040e4c08b0b8bcec767ce4a0

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

Using essentially the method for the intermediate of Example 12, starting from 3-(4(3(S)-aminopyrrolidin-1-yl)-3-fluorophenyl)-5(R)-(N-2,2,2-trichloroethyloxycarbonyl)isoxazol-3-ylaminomethyl)oxazolidin-2-one hydrochloride salt (419 mg, 0.73 mM) and 2-methoxyethyl chloroformate (450 mg, 3.27 mM) gave the title compound (442 mg).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07087629B2uspto-grants-2006_08