ethyl 4-(4-bromophenyl)-6-methyl-2-(piperidin-1-yl)pyrimidine-5-carboxylate

Base Information

Chemical Name:ethyl 4-(4-bromophenyl)-6-methyl-2-(piperidin-1-yl)pyrimidine-5-carboxylate
CAS No.:1245716-63-5
Molecular Formula:C₁₉H₂₂BrN₃O₂
Molecular Weight:404.307
Hs Code.:

Synonyms:ethyl 4-(4-bromophenyl)-6-methyl-2-(piperidin-1-yl)pyrimidine-5-carboxylate

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Chemical Property of ethyl 4-(4-bromophenyl)-6-methyl-2-(piperidin-1-yl)pyrimidine-5-carboxylate

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Technology Process of ethyl 4-(4-bromophenyl)-6-methyl-2-(piperidin-1-yl)pyrimidine-5-carboxylate

There total 5 articles about ethyl 4-(4-bromophenyl)-6-methyl-2-(piperidin-1-yl)pyrimidine-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: 85.0%

: 110-89-4
piperidine

: 1245716-72-6
C₁₄H₁₃BrN₂O₃

: 1245716-63-5
ethyl 4-(4-bromophenyl)-6-methyl-2-(piperidin-1-yl)pyrimidine-5-carboxylate

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 0 - 20 ℃; for 2.5h;
DOI:10.1016/j.tet.2011.02.046

Reference yield: 85.0%

: 110-89-4
piperidine

: ethyl 4-(4-bromophenyl)-2-[(diethoxyphosphoryl)oxy]-6-methylpyrimidine-5-carboxylate

: 1245716-63-5
ethyl 4-(4-bromophenyl)-6-methyl-2-(piperidin-1-yl)pyrimidine-5-carboxylate

Guidance literature:: at 60 ℃; for 1h;
DOI:10.1055/s-0035-1560175

Reference yield: 85.0%

: 110-89-4
piperidine

: 1606128-31-7
diethyl 2,2'-disulfanediylbis(4-(4-bromophenyl)-6-methylpyrimidine-5-carboxylate)

: 1245716-63-5
ethyl 4-(4-bromophenyl)-6-methyl-2-(piperidin-1-yl)pyrimidine-5-carboxylate

Guidance literature:: With potassium phosphate; copper(l) chloride; In 5,5-dimethyl-1,3-cyclohexadiene; at 140 ℃; for 8h; chemoselective reaction; Inert atmosphere; Schlenk technique;
DOI:10.1039/c5ob02535d