4-amino-6-((1-(3-phenyl-1,5-naphthyridin-2-yl)ethyl)amino)-5-pyrimidinecarbonitrile

Base Information

Chemical Name:4-amino-6-((1-(3-phenyl-1,5-naphthyridin-2-yl)ethyl)amino)-5-pyrimidinecarbonitrile
CAS No.:1312605-49-4
Molecular Formula:C₂₁H₁₇N₇
Molecular Weight:367.413
Hs Code.:

Synonyms:4-amino-6-((1-(3-phenyl-1,5-naphthyridin-2-yl)ethyl)amino)-5-pyrimidinecarbonitrile

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Chemical Property of 4-amino-6-((1-(3-phenyl-1,5-naphthyridin-2-yl)ethyl)amino)-5-pyrimidinecarbonitrile

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Technology Process of 4-amino-6-((1-(3-phenyl-1,5-naphthyridin-2-yl)ethyl)amino)-5-pyrimidinecarbonitrile

There total 8 articles about 4-amino-6-((1-(3-phenyl-1,5-naphthyridin-2-yl)ethyl)amino)-5-pyrimidinecarbonitrile 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:

: 1312605-81-4
1-(3-Phenyl-1,5-naphthyridin-2-yl)ethanamine

: 60025-09-4
4-amino-6-chloropyrimidine-5-carbonitrile

: 1312605-49-4
4-amino-6-((1-(3-phenyl-1,5-naphthyridin-2-yl)ethyl)amino)-5-pyrimidinecarbonitrile

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In butan-1-ol; at 130 ℃; for 4h;

Reference yield:

: 867353-50-2
2-chloro-3-phenyl-1,5-naphthyridine

: 1312605-49-4
4-amino-6-((1-(3-phenyl-1,5-naphthyridin-2-yl)ethyl)amino)-5-pyrimidinecarbonitrile

Guidance literature:: Multi-step reaction with 5 steps

1: potassium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / hexane; tetrahydrofuran / 6 h / Inert atmosphere; Reflux

2: 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione / dibenzoyl peroxide / tetrachloromethane / 3 h / Reflux

3: N,N-dimethyl-formamide / 2 h / 60 °C

4: hydrazine / ethanol / 0.5 h / 70 °C

5: N-ethyl-N,N-diisopropylamine / butan-1-ol / 4 h / 130 °C

With 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; potassium carbonate; N-ethyl-N,N-diisopropylamine; hydrazine; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; dibenzoyl peroxide; In tetrahydrofuran; tetrachloromethane; ethanol; hexane; N,N-dimethyl-formamide; butan-1-ol;

Reference yield:

: 1312605-78-9
2-Ethyl-3-phenyl-1,5-naphthyridine

: 1312605-49-4
4-amino-6-((1-(3-phenyl-1,5-naphthyridin-2-yl)ethyl)amino)-5-pyrimidinecarbonitrile

Guidance literature:: Multi-step reaction with 4 steps

1: 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione / dibenzoyl peroxide / tetrachloromethane / 3 h / Reflux

2: N,N-dimethyl-formamide / 2 h / 60 °C

3: hydrazine / ethanol / 0.5 h / 70 °C

4: N-ethyl-N,N-diisopropylamine / butan-1-ol / 4 h / 130 °C

With 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; N-ethyl-N,N-diisopropylamine; hydrazine; dibenzoyl peroxide; In tetrachloromethane; ethanol; N,N-dimethyl-formamide; butan-1-ol;