[4-[2-(3-hydroxyazetidin-1-yl)-pyrimidin-4-yl]-3-(3-methoxy-5-methylphenyl)-pyrazol-1-yl]acetonitrile

Base Information

Chemical Name:[4-[2-(3-hydroxyazetidin-1-yl)-pyrimidin-4-yl]-3-(3-methoxy-5-methylphenyl)-pyrazol-1-yl]acetonitrile
CAS No.:1262110-35-9
Molecular Formula:C₂₀H₂₀N₆O₂
Molecular Weight:376.418
Hs Code.:

Synonyms:[4-[2-(3-hydroxyazetidin-1-yl)-pyrimidin-4-yl]-3-(3-methoxy-5-methylphenyl)-pyrazol-1-yl]acetonitrile

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Chemical Property of [4-[2-(3-hydroxyazetidin-1-yl)-pyrimidin-4-yl]-3-(3-methoxy-5-methylphenyl)-pyrazol-1-yl]acetonitrile

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Technology Process of [4-[2-(3-hydroxyazetidin-1-yl)-pyrimidin-4-yl]-3-(3-methoxy-5-methylphenyl)-pyrazol-1-yl]acetonitrile

There total 7 articles about [4-[2-(3-hydroxyazetidin-1-yl)-pyrimidin-4-yl]-3-(3-methoxy-5-methylphenyl)-pyrazol-1-yl]acetonitrile 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: 57.3%

: 1262110-34-8
[4-(2-methanesulfonylpyrimidin-4-yl)-3-(3-methoxy-5-methylphenyl)-pyrazol-1-yl]acetonitrile

: 18621-18-6
azetion-3-ol hydrochloride

: 1262110-35-9
[4-[2-(3-hydroxyazetidin-1-yl)-pyrimidin-4-yl]-3-(3-methoxy-5-methylphenyl)-pyrazol-1-yl]acetonitrile

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 80 ℃; for 3h;

Reference yield:

: 585-81-9
3-hydroxy-5-methylbenzoic acid

: 1262110-35-9
[4-[2-(3-hydroxyazetidin-1-yl)-pyrimidin-4-yl]-3-(3-methoxy-5-methylphenyl)-pyrazol-1-yl]acetonitrile

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium carbonate / dmap / acetone / 12 h / 65 °C

2.1: lithium hexamethyldisilazane / tetrahydrofuran / 16 h / 20 °C

3.1: 20 h / 90 °C

3.2: 12 h / 20 °C

4.1: potassium carbonate / N,N-dimethyl-formamide / 16 h / 50 °C

5.1: magnesium sulfate; 3-chloro-benzenecarboperoxoic acid / dichloromethane / 2 h / 20 °C

6.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 3 h / 80 °C

With magnesium sulfate; potassium carbonate; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; lithium hexamethyldisilazane; dmap; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; acetone;

Reference yield:

: 14001-63-9
2-methylthio-4-methylpyrimidine

: 1262110-35-9
[4-[2-(3-hydroxyazetidin-1-yl)-pyrimidin-4-yl]-3-(3-methoxy-5-methylphenyl)-pyrazol-1-yl]acetonitrile

Guidance literature:: Multi-step reaction with 5 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran / 16 h / 20 °C

2.1: 20 h / 90 °C

2.2: 12 h / 20 °C

3.1: potassium carbonate / N,N-dimethyl-formamide / 16 h / 50 °C

4.1: magnesium sulfate; 3-chloro-benzenecarboperoxoic acid / dichloromethane / 2 h / 20 °C

5.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 3 h / 80 °C

With magnesium sulfate; potassium carbonate; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; lithium hexamethyldisilazane; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;