Reaction #2298622

ord-fa786f3772524887905c2d13b40f7ce8

Reaction equation

Clc1ncnc2c(Br)csc12
7-bromo-4-chlorothieno[3,2-d]pyrimidine
Clc1ncnc2c(Br)csc12
7-Bromo-4-chlorothieno[3,2-d]pyrimidine
NN.O
hydrazine monohydrate
Cl.NNc1ncnc2c(Br)csc12
(7-bromothieno[3,2-d]pyrimidin-4-yl) hydrazine hydrochloride
Yield 73.0%

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Temperaturewas heated
  2. 2
    Temperatureat reflux for 2 hour
  3. 3
    Filtrationthe solid product was collected by vacuum filtration

Procedure

A suspension of 7-bromo-4-chlorothieno[3,2-d]pyrimidine (159, 80 mg, 0.32 mmol) and hydrazine monohydrate (0.2 mL, 4.1 mmol) in ethanol (1.3 mL) was heated at reflux for 2 hour. After cooling to room temperature, the solid product was collected by vacuum filtration to give (7-bromothieno[3,2-d]pyrimidin-4-yl) hydrazine hydrochloride (57 mg, 73% yield) as a white solid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: USRE039267E1uspto-grants-2006_09