5-(2-((1-(3-chlorobenzyl)-1H-1,2,3-triazol-4-yl)methoxy)-4-methoxybenzoyl)-1-o-tolylpyridin-2(1H)-one

Base Information

Chemical Name:5-(2-((1-(3-chlorobenzyl)-1H-1,2,3-triazol-4-yl)methoxy)-4-methoxybenzoyl)-1-o-tolylpyridin-2(1H)-one
CAS No.:1388221-77-9
Molecular Formula:C₃₀H₂₅ClN₄O₄
Molecular Weight:541.006
Hs Code.:

Synonyms:5-(2-((1-(3-chlorobenzyl)-1H-1,2,3-triazol-4-yl)methoxy)-4-methoxybenzoyl)-1-o-tolylpyridin-2(1H)-one

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Chemical Property of 5-(2-((1-(3-chlorobenzyl)-1H-1,2,3-triazol-4-yl)methoxy)-4-methoxybenzoyl)-1-o-tolylpyridin-2(1H)-one

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Technology Process of 5-(2-((1-(3-chlorobenzyl)-1H-1,2,3-triazol-4-yl)methoxy)-4-methoxybenzoyl)-1-o-tolylpyridin-2(1H)-one

There total 8 articles about 5-(2-((1-(3-chlorobenzyl)-1H-1,2,3-triazol-4-yl)methoxy)-4-methoxybenzoyl)-1-o-tolylpyridin-2(1H)-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:

: 1388221-47-3
5-(4-methoxy-2-(prop-2-ynyloxy)benzoyl)-1-o-tolylpyridin-2(1H)-one

: 620-20-2,130468-19-8
1-Chloro-3-chloromethyl-benzene

: 1388221-77-9
5-(2-((1-(3-chlorobenzyl)-1H-1,2,3-triazol-4-yl)methoxy)-4-methoxybenzoyl)-1-o-tolylpyridin-2(1H)-one

Guidance literature:: With sodium azide; copper(ll) sulfate pentahydrate; sodium L-ascorbate; In acetone; at 20 ℃; for 2.5h;
DOI:10.1016/j.ejmech.2013.06.046

Reference yield:

: 552-41-0
1-(2-hydroxy-4-methoxyphenyl)ethanone

: 1388221-77-9
5-(2-((1-(3-chlorobenzyl)-1H-1,2,3-triazol-4-yl)methoxy)-4-methoxybenzoyl)-1-o-tolylpyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 8 steps

1: sodium / diethyl ether / 0 °C

2: acetic acid; hydrogenchloride / water / 0.5 h / 100 °C

3: methanol / Reflux

4: iodine / dichloromethane

5: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; potassium carbonate / water; tetrahydrofuran / 100 °C

6: methanol / Reflux

7: potassium carbonate / dichloromethane / 6 h / 20 °C

8: sodium azide; copper(ll) sulfate pentahydrate; sodium L-ascorbate / acetone / 2.5 h / 20 °C

With hydrogenchloride; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; sodium azide; copper(ll) sulfate pentahydrate; iodine; sodium; potassium carbonate; acetic acid; sodium L-ascorbate; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; water; acetone; 5: |Heck Reaction;
DOI:10.1016/j.ejmech.2013.06.046

Reference yield:

: 94719-81-0
ω-formyl-4'-methoxy-2'-hydroxyacetophenone

: 1388221-77-9
5-(2-((1-(3-chlorobenzyl)-1H-1,2,3-triazol-4-yl)methoxy)-4-methoxybenzoyl)-1-o-tolylpyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 7 steps

1: acetic acid; hydrogenchloride / water / 0.5 h / 100 °C

2: methanol / Reflux

3: iodine / dichloromethane

4: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; potassium carbonate / water; tetrahydrofuran / 100 °C

5: methanol / Reflux

6: potassium carbonate / dichloromethane / 6 h / 20 °C

7: sodium azide; copper(ll) sulfate pentahydrate; sodium L-ascorbate / acetone / 2.5 h / 20 °C

With hydrogenchloride; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; sodium azide; copper(ll) sulfate pentahydrate; iodine; potassium carbonate; acetic acid; sodium L-ascorbate; In tetrahydrofuran; methanol; dichloromethane; water; acetone; 4: |Heck Reaction;
DOI:10.1016/j.ejmech.2013.06.046