N-(5-chloro-2-{3-[3-(4-chlorobenzyl)-2-oxotetrahydropyrimidin-1(2H)-yl]-2-hydroxypropoxy}-4-methoxyphenyl)acetamide

Base Information

Chemical Name:N-(5-chloro-2-{3-[3-(4-chlorobenzyl)-2-oxotetrahydropyrimidin-1(2H)-yl]-2-hydroxypropoxy}-4-methoxyphenyl)acetamide
CAS No.:1076242-89-1
Molecular Formula:C₂₃H₂₇Cl₂N₃O₅
Molecular Weight:496.39
Hs Code.:

Synonyms:N-(5-chloro-2-{3-[3-(4-chlorobenzyl)-2-oxotetrahydropyrimidin-1(2H)-yl]-2-hydroxypropoxy}-4-methoxyphenyl)acetamide

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Chemical Property of N-(5-chloro-2-{3-[3-(4-chlorobenzyl)-2-oxotetrahydropyrimidin-1(2H)-yl]-2-hydroxypropoxy}-4-methoxyphenyl)acetamide

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Technology Process of N-(5-chloro-2-{3-[3-(4-chlorobenzyl)-2-oxotetrahydropyrimidin-1(2H)-yl]-2-hydroxypropoxy}-4-methoxyphenyl)acetamide

There total 3 articles about N-(5-chloro-2-{3-[3-(4-chlorobenzyl)-2-oxotetrahydropyrimidin-1(2H)-yl]-2-hydroxypropoxy}-4-methoxyphenyl)acetamide 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:

: 1076243-04-3
1-(4-chlorobenzyl)-3-(oxiran-2-ylmethyl)tetrahydropyrimidin-2(1H)-one

: 88581-06-0
acetic acid-(5-chloro-2-hydroxy-4-methoxy-anilide)

: 1076242-89-1
N-(5-chloro-2-{3-[3-(4-chlorobenzyl)-2-oxotetrahydropyrimidin-1(2H)-yl]-2-hydroxypropoxy}-4-methoxyphenyl)acetamide

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 120 ℃; for 3h;

Reference yield:

: 34790-85-7
1-(4-chlorobenzyl)hexahydropyrimidin-2-one

: 1076242-89-1
N-(5-chloro-2-{3-[3-(4-chlorobenzyl)-2-oxotetrahydropyrimidin-1(2H)-yl]-2-hydroxypropoxy}-4-methoxyphenyl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate / water / 0.08 h / 20 °C

1.2: 18 h / 20 °C

2.1: potassium carbonate / N,N-dimethyl-formamide / 3 h / 120 °C

With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; In water; N,N-dimethyl-formamide;

Reference yield:

: 622-95-7
4-chlorobenzyl bromide

: 1076242-89-1
N-(5-chloro-2-{3-[3-(4-chlorobenzyl)-2-oxotetrahydropyrimidin-1(2H)-yl]-2-hydroxypropoxy}-4-methoxyphenyl)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium tert-butylate / tetrahydrofuran / 0.75 h / 20 °C

1.2: 0.83 h / 0 - 20 °C

2.1: sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate / water / 0.08 h / 20 °C

2.2: 18 h / 20 °C

3.1: potassium carbonate / N,N-dimethyl-formamide / 3 h / 120 °C

With sodium hydroxide; potassium tert-butylate; tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; In tetrahydrofuran; water; N,N-dimethyl-formamide;