Reacción #2298616

ord-3da2c064d6f248c991c45bdc18310db0

Ecuación de reacción

Cc1csc2c(Cl)ncnc12
4-chloro-7-methylthieno[3,2-d]pyrimidine
Cc1csc2c(Cl)ncnc12
4-Chloro-7-methylthieno[3,2-d]pyrimidine
NN.O
hydrazine monohydrate
Cc1csc2c(NN)ncnc12.Cl
(7-methylthieno[3,2-d]pyrimidin-4-yl)hydrazine hydrochloride
Rendimiento 88.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawas heated
  2. 2
    Temperaturaat reflux for 1 hour
  3. 3
    Filtraciónthe solid product was collected by vacuum filtration

Procedimiento

A suspension of 4-chloro-7-methylthieno[3,2-d]pyrimidine (4, 3.1 g, 17 mmol) and hydrazine monohydrate (3.5 mL, 72 mmol) in ethanol (34 mL) was heated at reflux for 1 hour. After cooling to room temperature, the solid product was collected by vacuum filtration to give (7-methylthieno[3,2-d]pyrimidin-4-yl)hydrazine hydrochloride (3.2 g, 88% yield) as a white solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: USRE039267E1uspto-grants-2006_09