ethyl 4-((2-(benzylamino)-2-oxoethyl)amino)-2-phenylpyrimidine-5-carboxylate

Base Information

Chemical Name:ethyl 4-((2-(benzylamino)-2-oxoethyl)amino)-2-phenylpyrimidine-5-carboxylate
CAS No.:1149758-75-7
Molecular Formula:C₂₂H₂₂N₄O₃
Molecular Weight:390.442
Hs Code.:

Synonyms:ethyl 4-((2-(benzylamino)-2-oxoethyl)amino)-2-phenylpyrimidine-5-carboxylate

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Chemical Property of ethyl 4-((2-(benzylamino)-2-oxoethyl)amino)-2-phenylpyrimidine-5-carboxylate

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Technology Process of ethyl 4-((2-(benzylamino)-2-oxoethyl)amino)-2-phenylpyrimidine-5-carboxylate

There total 4 articles about ethyl 4-((2-(benzylamino)-2-oxoethyl)amino)-2-phenylpyrimidine-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: 91.0%

: 226954-91-2
2-(5-ethoxycarbonyl-2-phenylpyrimidine-4-ylamino)acetic acid

: 100-46-9
benzylamine

: 1149758-75-7
ethyl 4-((2-(benzylamino)-2-oxoethyl)amino)-2-phenylpyrimidine-5-carboxylate

Guidance literature:: With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 1h;
DOI:10.1002/bkcs.10979

Reference yield:

: 24755-82-6
ethyl 4-chloro-2-phenylpyrimidine-5-carboxylate

: 1149758-75-7
ethyl 4-((2-(benzylamino)-2-oxoethyl)amino)-2-phenylpyrimidine-5-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / ethanol / 4 h / 80 °C

2: triethylamine; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate / N,N-dimethyl-formamide / 1 h / 20 °C

With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In ethanol; N,N-dimethyl-formamide;
DOI:10.1002/bkcs.10979

Reference yield:

: 87-13-8
diethyl 2-ethoxymethylenemalonate

: 1149758-75-7
ethyl 4-((2-(benzylamino)-2-oxoethyl)amino)-2-phenylpyrimidine-5-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium ethanolate / ethanol / 0.5 h / 20 °C

1.2: 20 - 80 °C

2.1: trichlorophosphate / 4 h / 90 °C

3.1: triethylamine / ethanol / 4 h / 80 °C

4.1: triethylamine; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate / N,N-dimethyl-formamide / 1 h / 20 °C

With sodium ethanolate; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; trichlorophosphate; In ethanol; N,N-dimethyl-formamide;
DOI:10.1002/bkcs.10979