2-(2-bromo-4-isopropylanilino)-4-(5-phenyl-1,2,3,6-tetrahydropyridino)-6-methylpyrimidine

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Chemical Name:2-(2-bromo-4-isopropylanilino)-4-(5-phenyl-1,2,3,6-tetrahydropyridino)-6-methylpyrimidine
CAS No.:213923-83-2
Molecular Formula:C₂₅H₂₇BrN₄
Molecular Weight:463.42
Hs Code.:

Synonyms:2-(2-bromo-4-isopropylanilino)-4-(5-phenyl-1,2,3,6-tetrahydropyridino)-6-methylpyrimidine

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Chemical Property of 2-(2-bromo-4-isopropylanilino)-4-(5-phenyl-1,2,3,6-tetrahydropyridino)-6-methylpyrimidine

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Technology Process of 2-(2-bromo-4-isopropylanilino)-4-(5-phenyl-1,2,3,6-tetrahydropyridino)-6-methylpyrimidine

There total 5 articles about 2-(2-bromo-4-isopropylanilino)-4-(5-phenyl-1,2,3,6-tetrahydropyridino)-6-methylpyrimidine 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:

: 5424-21-5
2,4-dichloro-6-methylpyrimidine

: 213923-83-2
2-(2-bromo-4-isopropylanilino)-4-(5-phenyl-1,2,3,6-tetrahydropyridino)-6-methylpyrimidine

Guidance literature:: Multi-step reaction with 2 steps

1: 2.17 g / diisopropylethylamine / ethanol / -10 - 20 °C

2: 74 percent / diisopropylethylamine / ethane-1,2-diol / 1.5 h / Heating

With N-ethyl-N,N-diisopropylamine; In ethanol; ethylene glycol;
DOI:10.1016/S0968-0896(01)00004-9

Reference yield:

: 108-86-1,52753-63-6
bromobenzene

: 213923-83-2
2-(2-bromo-4-isopropylanilino)-4-(5-phenyl-1,2,3,6-tetrahydropyridino)-6-methylpyrimidine

Guidance literature:: Multi-step reaction with 4 steps

1.1: magnesium / tetrahydrofuran

1.2: 61 percent / tetrahydrofuran / 1.5 h

2.1: trifluoroacetic acid / Heating

3.1: 2.17 g / diisopropylethylamine / ethanol / -10 - 20 °C

4.1: 74 percent / diisopropylethylamine / ethane-1,2-diol / 1.5 h / Heating

With magnesium; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In tetrahydrofuran; ethanol; ethylene glycol;
DOI:10.1016/S0968-0896(01)00004-9

Reference yield:

: 98977-36-7
3-oxo-piperidine-1-carboxylic acid tert-butyl ester

: 213923-83-2
2-(2-bromo-4-isopropylanilino)-4-(5-phenyl-1,2,3,6-tetrahydropyridino)-6-methylpyrimidine

Guidance literature:: Multi-step reaction with 4 steps

1.1: magnesium / tetrahydrofuran

1.2: 61 percent / tetrahydrofuran / 1.5 h

2.1: trifluoroacetic acid / Heating

3.1: 2.17 g / diisopropylethylamine / ethanol / -10 - 20 °C

4.1: 74 percent / diisopropylethylamine / ethane-1,2-diol / 1.5 h / Heating

With magnesium; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In tetrahydrofuran; ethanol; ethylene glycol;
DOI:10.1016/S0968-0896(01)00004-9