Reaktion #2298628

ord-70ca48bfe13d4c889ae27b2e5898197b

Reaktionsgleichung

Cl.NNc1ncnc2cc(-c3ccsc3)sc12
(6-(3-thienyl)thieno[3,2-d]pyrimidin-4-yl)hydrazine hydrochloride
Cl.NNc1ncnc2cc(-c3ccsc3)sc12
(6-(3-Thienyl)thieno[3,2-d]pyrimidin-4-yl)hydrazine hydrochloride
O=Cc1cccnc1
3-pyridinecarboxaldehyde
C(=NNc1ncnc2cc(-c3ccsc3)sc12)c1cccnc1
3-pyridinecarboxaldehyde(6-(3-thienyl)thieno[3,2-d]pyrimidin-4-yl)hydrazone
Ausbeute 87.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas heated
  2. 2
    Temperaturat reflux for 4 hours
  3. 3
    Filtrationthe solid product was collected by vacuum filtration

Vorschrift

A suspension of (6-(3-thienyl)thieno[3,2-d]pyrimidin-4-yl)hydrazine hydrochloride (222, 39 mg, 0.14 mmol) and 3-pyridinecarboxaldehyde (20 mg, 0.19 mmol) in ethanol (2 mL) was heated at reflux for 4 hours. After cooling to room temperature, the solid product was collected by vacuum filtration to yield 3-pyridinecarboxaldehyde(6-(3-thienyl)thieno[3,2-d]pyrimidin-4-yl)hydrazone (40 mg, 87% yield) as a yellow solid.

Quelle

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