(R)-8-isopropyl-2-((1-methylpiperidin-4-yl)oxy)-N-(1-phenylethyl)pyrazolo[1,5-a][1,3,5]triazin-4-amine

Base Information

Chemical Name:(R)-8-isopropyl-2-((1-methylpiperidin-4-yl)oxy)-N-(1-phenylethyl)pyrazolo[1,5-a][1,3,5]triazin-4-amine
CAS No.:1453186-54-3
Molecular Formula:C₂₂H₃₀N₆O
Molecular Weight:394.52
Hs Code.:

Synonyms:(R)-8-isopropyl-2-((1-methylpiperidin-4-yl)oxy)-N-(1-phenylethyl)pyrazolo[1,5-a][1,3,5]triazin-4-amine

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Chemical Property of (R)-8-isopropyl-2-((1-methylpiperidin-4-yl)oxy)-N-(1-phenylethyl)pyrazolo[1,5-a][1,3,5]triazin-4-amine

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Technology Process of (R)-8-isopropyl-2-((1-methylpiperidin-4-yl)oxy)-N-(1-phenylethyl)pyrazolo[1,5-a][1,3,5]triazin-4-amine

There total 6 articles about (R)-8-isopropyl-2-((1-methylpiperidin-4-yl)oxy)-N-(1-phenylethyl)pyrazolo[1,5-a][1,3,5]triazin-4-amine 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:

: 1453186-75-8
4-chloro-8-isopropyl-2-((1-methylpiperidin-4-yl)oxy)pyrazolo[1,5-a] [1,3,5]triazine

: 3886-69-9
(R)-1-phenyl-ethyl-amine

: 1453186-54-3
(R)-8-isopropyl-2-((1-methylpiperidin-4-yl)oxy)-N-(1-phenylethyl)pyrazolo[1,5-a][1,3,5]triazin-4-amine

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In acetonitrile; at 0 - 20 ℃;

Reference yield:

: 1453186-94-1
8-isopropyl-2-thioxo-2,3-dihydropyrazolo[1,5-a][1,3,5]triazin-4(1H)-one

: 1453186-54-3
(R)-8-isopropyl-2-((1-methylpiperidin-4-yl)oxy)-N-(1-phenylethyl)pyrazolo[1,5-a][1,3,5]triazin-4-amine

Guidance literature:: Multi-step reaction with 5 steps

1: sodium hydroxide / ethanol; water / Cooling with ice

2: 3-chloro-benzenecarboperoxoic acid / dichloromethane

3: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 60 °C

4: N,N-diethylaniline; trichlorophosphate / 2 h / 80 °C

5: N-ethyl-N,N-diisopropylamine / acetonitrile / 0 - 20 °C

With sodium hydride; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; N,N-diethylaniline; sodium hydroxide; trichlorophosphate; In ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: ethyl N-[(4-isopropyl-1H-pyrazol-5-yl)carbamothioyl]carbamate

: 1453186-54-3
(R)-8-isopropyl-2-((1-methylpiperidin-4-yl)oxy)-N-(1-phenylethyl)pyrazolo[1,5-a][1,3,5]triazin-4-amine

Guidance literature:: Multi-step reaction with 6 steps

1: potassium carbonate / acetonitrile / 2 h / Reflux

2: sodium hydroxide / ethanol; water / Cooling with ice

3: 3-chloro-benzenecarboperoxoic acid / dichloromethane

4: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 60 °C

5: N,N-diethylaniline; trichlorophosphate / 2 h / 80 °C

6: N-ethyl-N,N-diisopropylamine / acetonitrile / 0 - 20 °C

With sodium hydride; potassium carbonate; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; N,N-diethylaniline; sodium hydroxide; trichlorophosphate; In ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;