Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

(E)-N-(4-chlorobenzylidene)-3-(4-chlorophenyl)-1H-pyrazole-5-carbohydrazide synthesis

3synthesis methods
890012-50-7 Synthesis
3-(4-CHLOROPHENYL)-1H-PYRAZOLE-5-CARBOHYDRAZIDE

890012-50-7
16 suppliers
inquiry

(E)-N-(4-chlorobenzylidene)-3-(4-chlorophenyl)-1H-pyrazole-5-carbohydrazide

1284275-59-7
5 suppliers
inquiry

-

Yield:1284275-59-7 60%

Reaction Conditions:

with acetic acid in methanol; for 6 h;Reflux;

Steps:

General procedure for the synthesis of hydrazones (4a-j)

General procedure: The hydrazones were prepared by condensation of hydrazide (10.0 mmol) and the appropriate aromatic aldehyde (10.5 mmol), in 55 ml of mixture of glacial CH3COOH:CH3OH (5:50) under reflux for 6 h. After cooling, the crude product was collected by filtration, washed and crystallized from hot ethanol to give a hydrazone (4a-j).

References:

Pathak, Ravindra B.;Chovatia;Parekh [Bioorganic and Medicinal Chemistry Letters,2012,vol. 22,# 15,p. 5129 - 5133] Location in patent:supporting information; experimental part