Reaktion #86563

ord-e96913f11f7342cd9d815cf13cf7bda3

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenThe mixture was concentrated

Vorschrift

To a solution of 7-(1-azidoethyl)-3-methyl-6-(4-methylphenyl)-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one (0.050 g, 0.15 mmol) in tetrahydrofuran (2 mL) was added 1.00 M of trimethylphosphine in tetrahydrofuran (0.23 mL, 0.23 mmol) and the mixture was stirred at room temperature for 1 hour. The mixture was concentrated to give the crude product (40 mg), which was used directly in next step. LCMS calculated for C16H18N3OS (M+H)+: m/z=300.1. Found: 300.1.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09434746B2uspto-grants-2016_09