Reaktion #1838237

ord-c61751cecaa24639a60c49363ad9a374

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenThe mixture was concentrated in vacuo

Vorschrift

A solution of tert-butyl 3-(3-(benzyloxycarbonyl)benzyl)-4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decane-8-carboxylate (913 mg, 1.646 mmol, 1 equiv) in 4M hydrogen chloride solution in dioxane was stirred at ambient temperature for 4-5 h. The mixture was concentrated in vacuo and the residue was lyophilized to afford the hydrogen chloride salt of the title compound as a cream solid (747 mg, quant); MS for C28H29N3O3 m/z 456.04 (M+H)+.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09156840B2uspto-grants-2015_10