反応 #2298627

ord-2021c7b2701a45e5b577371b2be751aa

反応方程式

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
収率 66.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度was heated
  2. 2
    温度at reflux for 1 hour
  3. 3
    ろ過the solid product was collected by vacuum filtration

実験手順

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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: USRE039267E1uspto-grants-2006_09