Reacción #619645

ord-8486b65b493f45e6914e672b9f49f043

Ecuación de reacción

O=c1[nH]cnc2ccsc12
Thieno[3,2-d]pyrimidin-4(3H)-one
BrBr
bromine
O=c1[nH]cnc2c(Br)csc12
title compound
O=c1[nH]cnc2c(Br)csc12
7-bromo-3H-thieno[3,2-d]pyrimidin-4-one

Reactivos

Ninguno

Disolventes

Condiciones de reacción

Temperatura
120°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe reaction mixture was cooled to room temperature
  2. 2
    workup.DISTILLATIONdistilled under reduced pressure
  3. 3
    Otroto remove acetic acid
  4. 4
    Otrothe solid thus obtained
  5. 5
    Filtraciónwas filtered
  6. 6
    Lavadowashed with ether
  7. 7
    Otrodried

Procedimiento

Thieno[3,2-d]pyrimidin-4(3H)-one (12.5 g) was dissolved in acetic acid (52 mL), and bromine (13 mL) was added thereto. The reaction mixture was stirred at 120° C. for 12 hours in a hermetically sealed reactor. The reaction mixture was cooled to room temperature and distilled under reduced pressure to remove acetic acid. The reaction mixture was placed in ice water, and the solid thus obtained was filtered and washed with ether, and dried to obtain the title compound (7.8 g).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08853213B2uspto-grants-2014_10