3-(4-Chlorphenyl)-2.5-dihydro-6-phenyl-4-pyridazincarbonsaeure-methylester

Base Information

Chemical Name:3-(4-Chlorphenyl)-2.5-dihydro-6-phenyl-4-pyridazincarbonsaeure-methylester
CAS No.:77588-71-7
Molecular Formula:C₁₈H₁₅ClN₂O₂
Molecular Weight:326.782
Hs Code.:

Synonyms:3-(4-Chlorphenyl)-2.5-dihydro-6-phenyl-4-pyridazincarbonsaeure-methylester

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Chemical Property of 3-(4-Chlorphenyl)-2.5-dihydro-6-phenyl-4-pyridazincarbonsaeure-methylester

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Technology Process of 3-(4-Chlorphenyl)-2.5-dihydro-6-phenyl-4-pyridazincarbonsaeure-methylester

There total 3 articles about 3-(4-Chlorphenyl)-2.5-dihydro-6-phenyl-4-pyridazincarbonsaeure-methylester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 85.0%

: 77596-92-0
α-(4-Chlorbenzoyl)-γ-oxobenzolbutansaeure-methylester

: 77588-71-7
3-(4-Chlorphenyl)-2.5-dihydro-6-phenyl-4-pyridazincarbonsaeure-methylester

Guidance literature:: With hydrazine hydrate; In acetic acid; for 4h; Ambient temperature;

Reference yield:

: 104-88-1
4-chlorobenzaldehyde

: 77588-71-7
3-(4-Chlorphenyl)-2.5-dihydro-6-phenyl-4-pyridazincarbonsaeure-methylester

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / triethylamine / 5-(2-hydroxyethyl)-3,4-dimethyl-1,3-thiazoliumiodide / ethanol / 14 h / 80 °C

2: 85 percent / N₂H₄*H₂O / acetic acid / 4 h / Ambient temperature

With hydrazine hydrate; triethylamine; 3,4-dimethyl-5-(2-hydroxyethyl)thiazolium iodide; In ethanol; acetic acid;

Reference yield:

: 14274-07-8,19522-25-9,19522-28-2
methyl 3-benzoylacrylate

: 77588-71-7
3-(4-Chlorphenyl)-2.5-dihydro-6-phenyl-4-pyridazincarbonsaeure-methylester

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / triethylamine / 5-(2-hydroxyethyl)-3,4-dimethyl-1,3-thiazoliumiodide / ethanol / 14 h / 80 °C

2: 85 percent / N₂H₄*H₂O / acetic acid / 4 h / Ambient temperature

With hydrazine hydrate; triethylamine; 3,4-dimethyl-5-(2-hydroxyethyl)thiazolium iodide; In ethanol; acetic acid;