1-{5-[4-(1-amino-cyclobutyl)-phenyl]-6-phenyl-5H-pyrrolo[3,2-d]pyrimidin-2-yl}-pyrrolidin-3-ol

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Chemical Name:1-{5-[4-(1-amino-cyclobutyl)-phenyl]-6-phenyl-5H-pyrrolo[3,2-d]pyrimidin-2-yl}-pyrrolidin-3-ol
CAS No.:1439396-50-5
Molecular Formula:C₂₆H₂₇N₅O
Molecular Weight:425.533
Hs Code.:

Synonyms:1-{5-[4-(1-amino-cyclobutyl)-phenyl]-6-phenyl-5H-pyrrolo[3,2-d]pyrimidin-2-yl}-pyrrolidin-3-ol

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Chemical Property of 1-{5-[4-(1-amino-cyclobutyl)-phenyl]-6-phenyl-5H-pyrrolo[3,2-d]pyrimidin-2-yl}-pyrrolidin-3-ol

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Technology Process of 1-{5-[4-(1-amino-cyclobutyl)-phenyl]-6-phenyl-5H-pyrrolo[3,2-d]pyrimidin-2-yl}-pyrrolidin-3-ol

There total 4 articles about 1-{5-[4-(1-amino-cyclobutyl)-phenyl]-6-phenyl-5H-pyrrolo[3,2-d]pyrimidin-2-yl}-pyrrolidin-3-ol 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:

: 1439396-52-7
(1-{4-[2-(3-hydroxy-pyrrolidin-1-yl)-6-phenyl-pyrrolo[3,2-d]pyrimidin-5-yl]-phenyl}-cyclobutyl)-carbamic acid tert-butyl ester

: 1439396-50-5
1-{5-[4-(1-amino-cyclobutyl)-phenyl]-6-phenyl-5H-pyrrolo[3,2-d]pyrimidin-2-yl}-pyrrolidin-3-ol

Guidance literature:: With hydrogenchloride; In ethyl acetate; at 0 - 20 ℃; for 4h; Inert atmosphere;

Reference yield:

: 536-74-3
phenylacetylene

: 1439396-50-5
1-{5-[4-(1-amino-cyclobutyl)-phenyl]-6-phenyl-5H-pyrrolo[3,2-d]pyrimidin-2-yl}-pyrrolidin-3-ol

Guidance literature:: Multi-step reaction with 4 steps

1: bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine / 2 h / 100 °C / Inert atmosphere

2: caesium carbonate; XPhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,4-dioxane / 4 h / 100 °C / Inert atmosphere; Microwave irradiation

3: potassium carbonate / 1-methyl-pyrrolidin-2-one / 130 °C / Inert atmosphere

4: hydrogenchloride / ethyl acetate / 4 h / 0 - 20 °C / Inert atmosphere

With hydrogenchloride; bis-triphenylphosphine-palladium(II) chloride; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; copper(l) iodide; potassium carbonate; caesium carbonate; triethylamine; XPhos; In 1,4-dioxane; 1-methyl-pyrrolidin-2-one; ethyl acetate;

Reference yield:

: 1439396-27-6
5-bromo-2-chloro-4-(phenylethynyl)pyrimidine

: 1439396-50-5
1-{5-[4-(1-amino-cyclobutyl)-phenyl]-6-phenyl-5H-pyrrolo[3,2-d]pyrimidin-2-yl}-pyrrolidin-3-ol

Guidance literature:: Multi-step reaction with 3 steps

1: caesium carbonate; XPhos; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,4-dioxane / 4 h / 100 °C / Inert atmosphere; Microwave irradiation

2: potassium carbonate / 1-methyl-pyrrolidin-2-one / 130 °C / Inert atmosphere

3: hydrogenchloride / ethyl acetate / 4 h / 0 - 20 °C / Inert atmosphere

With hydrogenchloride; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; potassium carbonate; caesium carbonate; XPhos; In 1,4-dioxane; 1-methyl-pyrrolidin-2-one; ethyl acetate;