Reaction #2298627

ord-2021c7b2701a45e5b577371b2be751aa

Reaction equation

Clc1ncnc2cc(-c3ccsc3)sc12
6-(3-thienyl)-4-chlorothieno[3,2-d]pyrimidine
Clc1ncnc2cc(-c3ccsc3)sc12
6-(3-Thienyl)-4-chlorothieno[3,2-d]pyrimidine
NN.O
hydrazine monohydrate
Cl.NNc1ncnc2cc(-c3ccsc3)sc12
(6-(3-thienyl)thieno[3,2-d]pyrimidin-4-yl) hydrazine hydrochloride
Yield 66.0%

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

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

Procedure

A suspension of 6-(3-thienyl)-4-chlorothieno[3,2-d]pyrimidine (220, 65 mg, 0.26 mmol) and hydrazine monohydrate (0.1 mL, 2.1 mmol) in ethanol (1 mL) was heated at reflux for 1 hour. After cooling to room temperature, the solid product was collected by vacuum filtration to give (6-(3-thienyl)thieno[3,2-d]pyrimidin-4-yl) hydrazine hydrochloride (48 mg, 66% yield) as a white solid.

Source

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