Lasri condensation

The Lasri condensation is an organic chemistry reaction where chalcone reacts with a hydrazone to furnish an azine and 3,5-diphenyl-1H-pyrazole. It is named after the Portuguese-Moroccan chemist Jamal Lasri.
Mechanism
The reaction is started with nucleophilic attack of the amino moiety of hydrazone 1 on the carbonyl group of 3 to produce the azine intermediate 1-((E)-1,3-diphenylallylidene)-2-(diarylmethylene)hydrazine. This asymmetrical azine then undergoes nucleophilic attack from its diaryl imino sp -carbon atom by the amino NH<sub>2</sub> moiety of hydrazone 1 to afford a second intermediate where the C(sp )—N bond is cleaved to furnish the symmetrical azine 2. The other product, 1,3-diphenyl-2-propenone hydrazone 3a, cyclizes to afford 2,3-dihydro-3,5-diphenyl-1H-pyrazole which is then rapidly dehydrogenated to yield 3,5-diphenyl-1H-pyrazole 4. In this reaction hydrazone 1 is a source of nitrogen for 3,5-diphenyl-1H-pyrazole 4. Additionally, the reaction does not require the use of any catalyst or promoter.

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