(S)-3-(1-((9H-purin-6-yl)amino)ethyl)-2-phenyl-8-(1H-pyrazol-4-yl)isoquinolin-1(2H)-one

Base Information

Chemical Name:(S)-3-(1-((9H-purin-6-yl)amino)ethyl)-2-phenyl-8-(1H-pyrazol-4-yl)isoquinolin-1(2H)-one
CAS No.:1350643-11-6
Molecular Formula:C₂₅H₂₀N₈O
Molecular Weight:448.487
Hs Code.:

Synonyms:(S)-3-(1-((9H-purin-6-yl)amino)ethyl)-2-phenyl-8-(1H-pyrazol-4-yl)isoquinolin-1(2H)-one

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Chemical Property of (S)-3-(1-((9H-purin-6-yl)amino)ethyl)-2-phenyl-8-(1H-pyrazol-4-yl)isoquinolin-1(2H)-one

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Technology Process of (S)-3-(1-((9H-purin-6-yl)amino)ethyl)-2-phenyl-8-(1H-pyrazol-4-yl)isoquinolin-1(2H)-one

There total 6 articles about (S)-3-(1-((9H-purin-6-yl)amino)ethyl)-2-phenyl-8-(1H-pyrazol-4-yl)isoquinolin-1(2H)-one 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:

: 763120-58-7
1H-pyrazole-4-boronic acid

: 1201438-56-3
(S)-3-(1-((9H-purin-6-yl)amino)ethyl)-8-chloro-2-phenylisoquinolin-1(2H)-one

: 1350643-11-6
(S)-3-(1-((9H-purin-6-yl)amino)ethyl)-2-phenyl-8-(1H-pyrazol-4-yl)isoquinolin-1(2H)-one

Guidance literature:: With sodium carbonate; catacxium A; palladium diacetate; In 1-methyl-pyrrolidin-2-one; at 160 ℃; for 3h; Inert atmosphere;

Reference yield:

: 62-53-3
aniline

: 1350643-11-6
(S)-3-(1-((9H-purin-6-yl)amino)ethyl)-2-phenyl-8-(1H-pyrazol-4-yl)isoquinolin-1(2H)-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 2 h / 20 °C

1.2: 2 h / 20 - 40 °C

2.1: n-butyllithium / hexane; tetrahydrofuran / 1 h / -30 - -10 °C / Inert atmosphere

2.2: 1 h / -30 - -10 °C / Inert atmosphere

2.3: 1 h / Reflux

3.1: triethylamine / butan-1-ol / 16 h / Reflux

4.1: hydrogenchloride; water / ethanol / 1 h / 20 °C

4.2: pH 8 - 9

5.1: sodium carbonate; catacxium A / palladium diacetate / 1-methyl-pyrrolidin-2-one / 3 h / 160 °C / Inert atmosphere

With hydrogenchloride; n-butyllithium; oxalyl dichloride; water; sodium carbonate; triethylamine; catacxium A; palladium diacetate; N,N-dimethyl-formamide; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; ethanol; hexane; dichloromethane; butan-1-ol;

Reference yield:

: 21327-86-6
2-chloro-6-methylbenzoic acid

: 1350643-11-6
(S)-3-(1-((9H-purin-6-yl)amino)ethyl)-2-phenyl-8-(1H-pyrazol-4-yl)isoquinolin-1(2H)-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 2 h / 20 °C

1.2: 2 h / 20 - 40 °C

2.1: n-butyllithium / hexane; tetrahydrofuran / 1 h / -30 - -10 °C / Inert atmosphere

2.2: 1 h / -30 - -10 °C / Inert atmosphere

2.3: 1 h / Reflux

3.1: triethylamine / butan-1-ol / 16 h / Reflux

4.1: hydrogenchloride; water / ethanol / 1 h / 20 °C

4.2: pH 8 - 9

5.1: sodium carbonate; catacxium A / palladium diacetate / 1-methyl-pyrrolidin-2-one / 3 h / 160 °C / Inert atmosphere

With hydrogenchloride; n-butyllithium; oxalyl dichloride; water; sodium carbonate; triethylamine; catacxium A; palladium diacetate; N,N-dimethyl-formamide; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; ethanol; hexane; dichloromethane; butan-1-ol;