2-[2-(4-bromomethyl-2-methyl-phenyl)-2-oxo-ethyl]-5-(5-chloro-pyridin-2-ylmethoxy)-2H-pyridazin-3-one

Base Information

Chemical Name:2-[2-(4-bromomethyl-2-methyl-phenyl)-2-oxo-ethyl]-5-(5-chloro-pyridin-2-ylmethoxy)-2H-pyridazin-3-one
CAS No.:1453500-10-1
Molecular Formula:C₂₀H₁₇BrClN₃O₃
Molecular Weight:462.73
Hs Code.:

Synonyms:2-[2-(4-bromomethyl-2-methyl-phenyl)-2-oxo-ethyl]-5-(5-chloro-pyridin-2-ylmethoxy)-2H-pyridazin-3-one

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Chemical Property of 2-[2-(4-bromomethyl-2-methyl-phenyl)-2-oxo-ethyl]-5-(5-chloro-pyridin-2-ylmethoxy)-2H-pyridazin-3-one

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Technology Process of 2-[2-(4-bromomethyl-2-methyl-phenyl)-2-oxo-ethyl]-5-(5-chloro-pyridin-2-ylmethoxy)-2H-pyridazin-3-one

There total 9 articles about 2-[2-(4-bromomethyl-2-methyl-phenyl)-2-oxo-ethyl]-5-(5-chloro-pyridin-2-ylmethoxy)-2H-pyridazin-3-one 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:

: 1453500-09-8
5-(5-chloro-pyridin-2-ylmethoxy)-2-[2-(4-hydroxymethyl-2-methyl-phenyl)-2-oxo-ethyl]-2H-pyridazin-3-one

: 1453500-10-1
2-[2-(4-bromomethyl-2-methyl-phenyl)-2-oxo-ethyl]-5-(5-chloro-pyridin-2-ylmethoxy)-2H-pyridazin-3-one

Guidance literature:: With phosphorus tribromide; In dichloromethane; at 20 ℃;
DOI:10.1016/j.bmcl.2015.05.065

Reference yield:

: 1453499-96-1
2-bromo-1-(4-hydroxymethyl-2-methyl-phenyl)-ethanone

: 1453500-10-1
2-[2-(4-bromomethyl-2-methyl-phenyl)-2-oxo-ethyl]-5-(5-chloro-pyridin-2-ylmethoxy)-2H-pyridazin-3-one

Guidance literature:: Multi-step reaction with 2 steps

1: caesium carbonate

2: phosphorus tribromide / dichloromethane / 20 °C

With phosphorus tribromide; caesium carbonate; In dichloromethane;
DOI:10.1016/j.bmcl.2015.05.065

Reference yield:

: 149104-89-2
4-bromo-3-methylbenzylalcohol

: 1453500-10-1
2-[2-(4-bromomethyl-2-methyl-phenyl)-2-oxo-ethyl]-5-(5-chloro-pyridin-2-ylmethoxy)-2H-pyridazin-3-one

Guidance literature:: Multi-step reaction with 6 steps

1: copper(l) iodide; sodium iodide; N,N`-dimethylethylenediamine / 1,4-dioxane / 120 °C

2: potassium carbonate; palladium diacetate; 1,3-bis-(diphenylphosphino)propane; lithium chloride / N,N-dimethyl-formamide; water / 90 °C

3: hydrogenchloride / water / 20 °C

4: tetra-N-butylammonium tribromide / dichloromethane; methanol / 20 °C

5: caesium carbonate

6: phosphorus tribromide / dichloromethane / 20 °C

With hydrogenchloride; copper(l) iodide; 1,3-bis-(diphenylphosphino)propane; palladium diacetate; tetra-N-butylammonium tribromide; phosphorus tribromide; potassium carbonate; caesium carbonate; sodium iodide; lithium chloride; N,N`-dimethylethylenediamine; In 1,4-dioxane; methanol; dichloromethane; water; N,N-dimethyl-formamide; 2: |Heck Reaction;
DOI:10.1016/j.bmcl.2015.05.065