ethyl <5-<(2'-cyanobiphenyl-4-yl)methyl>-2-methyl-4-oxo-6-n-propylpyrimidin-3-yl>acetate

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Chemical Name:ethyl <5-<(2'-cyanobiphenyl-4-yl)methyl>-2-methyl-4-oxo-6-n-propylpyrimidin-3-yl>acetate
CAS No.:141309-98-0
Molecular Formula:C₂₆H₂₇N₃O₃
Molecular Weight:429.519
Hs Code.:

Synonyms:ethyl <5-<(2'-cyanobiphenyl-4-yl)methyl>-2-methyl-4-oxo-6-n-propylpyrimidin-3-yl>acetate

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Chemical Property of ethyl <5-<(2'-cyanobiphenyl-4-yl)methyl>-2-methyl-4-oxo-6-n-propylpyrimidin-3-yl>acetate

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Technology Process of ethyl <5-<(2'-cyanobiphenyl-4-yl)methyl>-2-methyl-4-oxo-6-n-propylpyrimidin-3-yl>acetate

There total 3 articles about ethyl <5-<(2'-cyanobiphenyl-4-yl)methyl>-2-methyl-4-oxo-6-n-propylpyrimidin-3-yl>acetate 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:

: 114772-54-2
4'-(bromomethyl)-1,1'-biphenyl-2-carbonitrile

: 141309-98-0
ethyl <5-<(2'-cyanobiphenyl-4-yl)methyl>-2-methyl-4-oxo-6-n-propylpyrimidin-3-yl>acetate

Guidance literature:: Multi-step reaction with 3 steps

1: N,N-diisopropylethylamine, LiCl / tetrahydrofuran / 15 h / Heating

2: 1.) NaOMe / 1.) MeOH, RT, 15 min, 2.) MeOH, a) 20 h RT, b) reflux, 3 h

3: 1.) NaH / 1.) DMF, 50 deg C, 30 min, 2.) DMF, a) RT, 3 h, b) 70 deg C, 1 h

With sodium methylate; sodium hydride; N-ethyl-N,N-diisopropylamine; lithium chloride; In tetrahydrofuran;
DOI:10.1016/0223-5234(96)88246-8

Reference yield:

: 3249-68-1
ethyl butyroyl acetate

: 141309-98-0
ethyl <5-<(2'-cyanobiphenyl-4-yl)methyl>-2-methyl-4-oxo-6-n-propylpyrimidin-3-yl>acetate

Guidance literature:: Multi-step reaction with 3 steps

1: N,N-diisopropylethylamine, LiCl / tetrahydrofuran / 15 h / Heating

2: 1.) NaOMe / 1.) MeOH, RT, 15 min, 2.) MeOH, a) 20 h RT, b) reflux, 3 h

3: 1.) NaH / 1.) DMF, 50 deg C, 30 min, 2.) DMF, a) RT, 3 h, b) 70 deg C, 1 h

With sodium methylate; sodium hydride; N-ethyl-N,N-diisopropylamine; lithium chloride; In tetrahydrofuran;
DOI:10.1016/0223-5234(96)88246-8

Reference yield:

: 105-36-2
ethyl bromoacetate

: 135689-67-7
5-<(2'-cyanobiphenyl-4-yl)methyl>-2-methyl-6-n-propylpyrimidin-4(3H)-one

: 141309-98-0
ethyl <5-<(2'-cyanobiphenyl-4-yl)methyl>-2-methyl-4-oxo-6-n-propylpyrimidin-3-yl>acetate

Guidance literature:: With sodium hydride; Yield given. Multistep reaction; 1.) DMF, 50 deg C, 30 min, 2.) DMF, a) RT, 3 h, b) 70 deg C, 1 h;
DOI:10.1016/0223-5234(96)88246-8