Reaction #1102747

ord-e3c6893f43c8401e867694940d3cad41

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Otherthe volatiles were removed under reduced pressure
  2. 2
    Otherthe residue was triturated several times with ether

Procedure

To a stirred solution of the compound obtained from example 19 (36 mg, 0.1 mmol) in methanol (2 mL) cooled to 0° C. was added TMS-Cl (25 μL, 0.2 mmol). After 30 minutes, the volatiles were removed under reduced pressure and the residue was triturated several times with ether to obtain the hydrochloride salt of (2S)-1-{N-[2-(2-oxopyrrolidin-1-yl)hexahydro-2,5-methanopentalen-3a(1H)-yl]glycyl}pyrrolidine-2-carbonitrile as off-white solid (38 mg).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07985759B2uspto-grants-2011_07