4-((4-(1-(4-bromophenyl)-1-hydroxyallyl)pyrimidin-2-yl)amino)benzonitrile

Base Information

Chemical Name:4-((4-(1-(4-bromophenyl)-1-hydroxyallyl)pyrimidin-2-yl)amino)benzonitrile
CAS No.:1601456-94-3
Molecular Formula:C₂₀H₁₅BrN₄O
Molecular Weight:407.269
Hs Code.:

Synonyms:4-((4-(1-(4-bromophenyl)-1-hydroxyallyl)pyrimidin-2-yl)amino)benzonitrile

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Chemical Property of 4-((4-(1-(4-bromophenyl)-1-hydroxyallyl)pyrimidin-2-yl)amino)benzonitrile

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Technology Process of 4-((4-(1-(4-bromophenyl)-1-hydroxyallyl)pyrimidin-2-yl)amino)benzonitrile

There total 4 articles about 4-((4-(1-(4-bromophenyl)-1-hydroxyallyl)pyrimidin-2-yl)amino)benzonitrile 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: 57.0%

: 1225464-94-7
2-(4-cyanophenylamino)-4-(4-bromobenzoyl)pyrimidine

: 3536-96-7
vinylmagnesium chloride

: 1601456-94-3
4-((4-(1-(4-bromophenyl)-1-hydroxyallyl)pyrimidin-2-yl)amino)benzonitrile

Guidance literature:: In tetrahydrofuran; at -20 - 20 ℃; for 2h; Inert atmosphere;
DOI:10.1016/j.bmc.2014.02.030

Reference yield:

: 4-[(1,4-dihydro-4-oxo-2-pyrimidinyl)amino]benzonitrile

: 1601456-94-3
4-((4-(1-(4-bromophenyl)-1-hydroxyallyl)pyrimidin-2-yl)amino)benzonitrile

Guidance literature:: Multi-step reaction with 4 steps

1: trichlorophosphate / 0.5 h / Reflux

2: sodium hydride / N,N-dimethyl-formamide / -20 - 20 °C / Inert atmosphere

3: air / 20 °C

4: tetrahydrofuran / 2 h / -20 - 20 °C / Inert atmosphere

With sodium hydride; trichlorophosphate; In tetrahydrofuran; N,N-dimethyl-formamide; 4: |Grignard Reaction;
DOI:10.1016/j.bmc.2014.02.030

Reference yield:

: 1232684-01-3
C₁₉H₁₂BrN₅

: 1601456-94-3
4-((4-(1-(4-bromophenyl)-1-hydroxyallyl)pyrimidin-2-yl)amino)benzonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: air / 20 °C

2: tetrahydrofuran / 2 h / -20 - 20 °C / Inert atmosphere

With air; In tetrahydrofuran; 2: |Grignard Reaction;
DOI:10.1016/j.bmc.2014.02.030