N-(3-chlorophenyl)-1-(2-phenylethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

Base Information

Chemical Name:N-(3-chlorophenyl)-1-(2-phenylethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine
CAS No.:1338789-10-8
Molecular Formula:C₁₉H₁₆ClN₅
Molecular Weight:349.823
Hs Code.:

Synonyms:N-(3-chlorophenyl)-1-(2-phenylethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

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Chemical Property of N-(3-chlorophenyl)-1-(2-phenylethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

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Technology Process of N-(3-chlorophenyl)-1-(2-phenylethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

There total 8 articles about N-(3-chlorophenyl)-1-(2-phenylethyl)-1H-pyrazolo[3,4-d]pyrimidin-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: 67.0%

: 1338789-23-3
N-(3-chlorophenyl)-6-(methylthio)-1-(2-phenylethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

: 1338789-10-8
N-(3-chlorophenyl)-1-(2-phenylethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

Guidance literature:: With 10 wt% Pd(OH)2 on carbon; hydrogen; In methanol; at 20 ℃; for 2h;
DOI:10.1021/co500004e

Reference yield: 61.0%

: 1338789-08-4
4-chloro-1-(2-phenylethyl)-1H-pyrazolo[3,4-d]pyrimidine

: 108-42-9
3-chloro-aniline

: 1338789-10-8
N-(3-chlorophenyl)-1-(2-phenylethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

Guidance literature:: In ethanol; Reflux;
DOI:10.1016/j.bmcl.2011.07.079

Reference yield:

: 33097-11-9
4,6-dichloro-2-methylsulfanylpyrimidine-5-carboxyaldehyde

: 1338789-10-8
N-(3-chlorophenyl)-1-(2-phenylethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine; hydrazine hydrate / 1,4-dioxane / 5 h / 20 °C

2: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 4 - 100 °C / Cooling with ice; Inert atmosphere; Microwave irradiation

3: ethanol / 12 h / Reflux; Inert atmosphere

4: 10 wt% Pd(OH)2 on carbon; hydrogen / methanol / 2 h / 20 °C

With di-isopropyl azodicarboxylate; 10 wt% Pd(OH)2 on carbon; hydrogen; hydrazine hydrate; triethylamine; triphenylphosphine; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol;
DOI:10.1021/co500004e