Reacción #1481462

ord-3b76e4d5c374488c8fee4a9af73c889b

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónThe resultant solid was filtered out
  2. 2
    Lavadowashed with ether (3×3 ml)
  3. 3
    Otrodried

Procedimiento

In order to produce the citrate, the more nonpolar diastereoisomer of 1-(4-dimethylamino-4-phenylcyclohexylmethyl)-3-[2-(1H-indol-3-yl)-1-methylethyl]-thiourea (167 mg, 0.37 mmole) was dissolved in ethanol (4 ml) at RT and combined with a solution of citric acid (78.7 mg, 0.41 mmole) in ethanol (1 ml). After 1 h, a tacky precipitate could be seen on the flask wall and was detached mechanically. The batch was then combined with ether (35 ml) and stirred for 20 h. The resultant solid was filtered out, washed with ether (3×3 ml) and dried. The nonpolar diastereoisomer of 1-(4-dimethylamino-4-phenyl-cyclohexylmethyl)-3-[2-(1H-indol-3-yl)-1-methylethyl]thiourea citrate was obtained in this way as a colorless solid (Example 39) in a yield of 206 mg (87%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07348354B2uspto-grants-2008_03