5-methyl-7-(4-methanesulfonylphenyl)-4-(piperidin-4-yloxy)-5H-pyrrolo[3,2-d]pyrimidine

Base Information

Chemical Name:5-methyl-7-(4-methanesulfonylphenyl)-4-(piperidin-4-yloxy)-5H-pyrrolo[3,2-d]pyrimidine
CAS No.:1384950-69-9
Molecular Formula:C₁₉H₂₂N₄O₃S
Molecular Weight:386.475
Hs Code.:

Synonyms:5-methyl-7-(4-methanesulfonylphenyl)-4-(piperidin-4-yloxy)-5H-pyrrolo[3,2-d]pyrimidine

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Chemical Property of 5-methyl-7-(4-methanesulfonylphenyl)-4-(piperidin-4-yloxy)-5H-pyrrolo[3,2-d]pyrimidine

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Technology Process of 5-methyl-7-(4-methanesulfonylphenyl)-4-(piperidin-4-yloxy)-5H-pyrrolo[3,2-d]pyrimidine

There total 7 articles about 5-methyl-7-(4-methanesulfonylphenyl)-4-(piperidin-4-yloxy)-5H-pyrrolo[3,2-d]pyrimidine 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:

: 1384950-68-8
tert-butyl 4-(5-methyl-7-(4-methanesulfonylphenyl)-5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)piperidin-1-carboxylate

: 1384950-69-9
5-methyl-7-(4-methanesulfonylphenyl)-4-(piperidin-4-yloxy)-5H-pyrrolo[3,2-d]pyrimidine

Guidance literature:: With trifluoroacetic acid; In dichloromethane; for 1h;

Reference yield:

: 5655-01-6
9-deazahypoxanthine

: 1384950-69-9
5-methyl-7-(4-methanesulfonylphenyl)-4-(piperidin-4-yloxy)-5H-pyrrolo[3,2-d]pyrimidine

Guidance literature:: Multi-step reaction with 6 steps

1.1: trichlorophosphate / Reflux

2.1: N-Bromosuccinimide / tetrahydrofuran / 1 h

3.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h

3.2: 2 h / 50 °C

4.1: potassium carbonate / N,N-dimethyl-formamide / 12 h / 100 °C / Sealed reactor

5.1: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane / 12 h / 100 °C / Sealed reactor

6.1: trifluoroacetic acid / dichloromethane / 1 h

With N-Bromosuccinimide; sodium hydride; potassium carbonate; trifluoroacetic acid; trichlorophosphate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 84905-80-6
4-Chloro-5H-pyrrolo[3,2-d]pyrimidine

: 1384950-69-9
5-methyl-7-(4-methanesulfonylphenyl)-4-(piperidin-4-yloxy)-5H-pyrrolo[3,2-d]pyrimidine

Guidance literature:: Multi-step reaction with 4 steps

1.1: N-Bromosuccinimide / tetrahydrofuran / 1 h

2.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h

2.2: 2 h / 50 °C

3.1: potassium carbonate / N,N-dimethyl-formamide / 12 h / 100 °C / Sealed reactor

4.1: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane / 12 h / 100 °C / Sealed reactor

With N-Bromosuccinimide; sodium hydride; potassium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl-formamide;