Reacción #159176

ord-bec1896fd7ad48a28e99653db7d86ac8

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Concentraciónthen concentrated
  2. 2
    OtroThe crude residue was purified by silica column chromatography (14% to 35% EtOAc/Hex)

Procedimiento

Crude 2-Bromo-1-(3a,6a-dihydro-thieno[3,2-b]thiophen-2-yl)-ethanone (2.48 mmol assuming complete conversion from starting material) was treated with Boc-proline and MeCN (25 mL). Triethylamine was added and the solution was stirred at RT for 1 h then concentrated. The crude residue was purified by silica column chromatography (14% to 35% EtOAc/Hex) to afford the title compound (595 mg, 61%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08822430B2uspto-grants-2014_09