ethyl 6-{[(6-tert-butyl-3-cyano-5,6,7,8-tetrahydroquinolin-2-yl)thio]methyl}-4-(4-methoxyphenyl)-1-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate

Base Information

Chemical Name:ethyl 6-{[(6-tert-butyl-3-cyano-5,6,7,8-tetrahydroquinolin-2-yl)thio]methyl}-4-(4-methoxyphenyl)-1-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate
CAS No.:1414778-43-0
Molecular Formula:C₃₀H₃₆N₄O₄S
Molecular Weight:548.706
Hs Code.:

ethyl 6-{[(6-tert-butyl-3-cyano-5,6,7,8-tetrahydroquinolin-2-yl)thio]methyl}-4-(4-methoxyphenyl)-1-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate

Synonyms:ethyl 6-{[(6-tert-butyl-3-cyano-5,6,7,8-tetrahydroquinolin-2-yl)thio]methyl}-4-(4-methoxyphenyl)-1-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate

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Chemical Property of ethyl 6-{[(6-tert-butyl-3-cyano-5,6,7,8-tetrahydroquinolin-2-yl)thio]methyl}-4-(4-methoxyphenyl)-1-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate

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Technology Process of ethyl 6-{[(6-tert-butyl-3-cyano-5,6,7,8-tetrahydroquinolin-2-yl)thio]methyl}-4-(4-methoxyphenyl)-1-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate

There total 4 articles about ethyl 6-{[(6-tert-butyl-3-cyano-5,6,7,8-tetrahydroquinolin-2-yl)thio]methyl}-4-(4-methoxyphenyl)-1-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate 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: 74.0%

: 728016-33-9
ethyl 6-(bromomethyl)-4-(4-methoxyphenyl)-1-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate

: 401631-92-3
6-tert-butyl-2-thioxo-1,2,5,6,7,8-hexahydroquinoline-3-carbonitrile

: 1414778-43-0
ethyl 6-{[(6-tert-butyl-3-cyano-5,6,7,8-tetrahydroquinolin-2-yl)thio]methyl}-4-(4-methoxyphenyl)-1-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate

Guidance literature:: 6-tert-butyl-2-thioxo-1,2,5,6,7,8-hexahydroquinoline-3-carbonitrile; With potassium hydroxide; In water; N,N-dimethyl-formamide; for 0.166667h;

ethyl 6-(bromomethyl)-4-(4-methoxyphenyl)-1-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate; In water; N,N-dimethyl-formamide; at 50 - 70 ℃; regioselective reaction;
DOI:10.1016/j.tet.2012.09.041

Reference yield:

: 219814-75-2
ethyl 4-(4-methoxyphenyl)-1,6-dimethyl-2-oxo-1,2,3,4-tetrahydropyrimidin-5-carboxylate

: 1414778-43-0
ethyl 6-{[(6-tert-butyl-3-cyano-5,6,7,8-tetrahydroquinolin-2-yl)thio]methyl}-4-(4-methoxyphenyl)-1-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: bromine

2.1: potassium hydroxide / water; N,N-dimethyl-formamide / 0.17 h

2.2: 50 - 70 °C

With bromine; potassium hydroxide; In water; N,N-dimethyl-formamide;
DOI:10.1016/j.tet.2012.09.041

Reference yield:

: 98-53-3
4-tercbutyl-cyclohexanone

: 1414778-43-0
ethyl 6-{[(6-tert-butyl-3-cyano-5,6,7,8-tetrahydroquinolin-2-yl)thio]methyl}-4-(4-methoxyphenyl)-1-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium tert-butylate / 30 h / 4 °C / Cooling with ice

2.1: acetic acid / ethanol / 6 h / 20 °C / Reflux

3.1: potassium hydroxide / water; N,N-dimethyl-formamide / 0.17 h

3.2: 50 - 70 °C

With potassium tert-butylate; acetic acid; potassium hydroxide; In ethanol; water; N,N-dimethyl-formamide;
DOI:10.1016/j.tet.2012.09.041