Reacción #2065001

ord-bcee8c91978942e7b091bac73cb36e5d

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónThe precipitate is filtered off with suction
  2. 2
    Lavadowashed with acetone
  3. 3
    Otrodried in vacuo

Procedimiento

1.06 g of 2-bromo-6-(4-trifluoromethylphenyl)indan-1-one are dissolved with 266 mg of thiourea in 10 ml of dry acetone and stirred at ice-bath temperature for 4 h. The precipitate is filtered off with suction, washed with acetone and dried in vacuo. The hydrobromide of 2-amino-5-(4-trifluoromethylphenyl)-8,8a-dihydroindeno[1,2-d]thiazol-3a-ol is obtained with a melting point of 228-230° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06235763B1uspto-grants-2001_05