Reacción #1586

ord-5c5c39356f4c47209692dae46b65a52e

Ecuación de reacción

Cl.O=C(c1ccc(OCCN2CCCCC2)cc1)c1c(-c2ccc(O)cc2)sc2cc(O)ccc12
Raloxifene HCl
CCN(CC)CC
triethylamine
CC/C=C/C/C=C/C/C=C/CCCCCCCC(=O)Cl
linolenoyl chloride
O=C(c1ccc(OCCN2CCCCC2)cc1)c1c(-c2ccc(O)cc2)sc2cc(O)ccc12
Raloxifene

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThis derivative was prepared in a manner similar to Example 1
  2. 2
    OtroThe final product was chromatographed on a silica gel column
  3. 3
    Lavadoeluted with EtOAc-hexane (8:2)

Procedimiento

This derivative was prepared in a manner similar to Example 1, using 2.6 g (0.005 mol) of Raloxifene HCl, 2 g (0.02 mol) of triethylamine, 20 mg of DMAP, and 3.2 g (0.01 mol) of linolenoyl chloride in 250 mL of THF. The final product was chromatographed on a silica gel column eluted with EtOAc-hexane (8:2). This yielded 3.21 g of the title compound as clear oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05726168uspto-grants-1998_03