6-(4-(1-aminocyclobutyl)phenyl)-3-(2-methoxyethyl)-2-(methylthio)-5-phenylfuro[2,3-d]pyrimidin-4(3H)-one hydrochloride

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Chemical Name:6-(4-(1-aminocyclobutyl)phenyl)-3-(2-methoxyethyl)-2-(methylthio)-5-phenylfuro[2,3-d]pyrimidin-4(3H)-one hydrochloride
CAS No.:1301609-41-5
Molecular Formula:C₂₆H₂₇N₃O₃S*ClH
Molecular Weight:498.046
Hs Code.:

Synonyms:6-(4-(1-aminocyclobutyl)phenyl)-3-(2-methoxyethyl)-2-(methylthio)-5-phenylfuro[2,3-d]pyrimidin-4(3H)-one hydrochloride

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Chemical Property of 6-(4-(1-aminocyclobutyl)phenyl)-3-(2-methoxyethyl)-2-(methylthio)-5-phenylfuro[2,3-d]pyrimidin-4(3H)-one hydrochloride

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Technology Process of 6-(4-(1-aminocyclobutyl)phenyl)-3-(2-methoxyethyl)-2-(methylthio)-5-phenylfuro[2,3-d]pyrimidin-4(3H)-one hydrochloride

There total 6 articles about 6-(4-(1-aminocyclobutyl)phenyl)-3-(2-methoxyethyl)-2-(methylthio)-5-phenylfuro[2,3-d]pyrimidin-4(3H)-one hydrochloride 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: 68.0%

: 1301611-61-9
tert-butyl 1-(4-(3-(2-methoxyethyl)-2-(methylthio)-4-oxo-5-phenyl-3,4-dihydrofuro[2,3-d]pyrimidin-6-yl)phenyl)cyclobutylcarbamate

: 1301609-41-5
6-(4-(1-aminocyclobutyl)phenyl)-3-(2-methoxyethyl)-2-(methylthio)-5-phenylfuro[2,3-d]pyrimidin-4(3H)-one hydrochloride

Guidance literature:: With hydrogenchloride; In tetrahydrofuran; 1,4-dioxane; at 20 ℃; for 3h;

Reference yield:

: 10428-49-6
β-chloro-β-nitrostyrene

: 1301609-41-5
6-(4-(1-aminocyclobutyl)phenyl)-3-(2-methoxyethyl)-2-(methylthio)-5-phenylfuro[2,3-d]pyrimidin-4(3H)-one hydrochloride

Guidance literature:: Multi-step reaction with 5 steps

1: 1,8-diazabicyclo[5.4.0]undec-7-ene / ethanol / 96 h / Inert atmosphere; Reflux

2: N-Bromosuccinimide; potassium acetate / N,N-dimethyl-formamide / 80 °C / Inert atmosphere; Sealed tube

3: sodium iodide / N,N-dimethyl-formamide / 3 h / 80 °C

4: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,2-dimethoxyethane; water / Reflux

5: hydrogenchloride / 1,4-dioxane; tetrahydrofuran / 3 h / 20 °C

With hydrogenchloride; N-Bromosuccinimide; potassium acetate; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; sodium iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; 1,2-dimethoxyethane; ethanol; water; N,N-dimethyl-formamide;

Reference yield:

: 1301611-59-5
6-bromo-3-(2-methoxyethyl)-2-(methylthio)-5-phenylfuro[2,3-d]pyrimidin-4(3H)-one

: 1301609-41-5
6-(4-(1-aminocyclobutyl)phenyl)-3-(2-methoxyethyl)-2-(methylthio)-5-phenylfuro[2,3-d]pyrimidin-4(3H)-one hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,2-dimethoxyethane; water / Reflux

2: hydrogenchloride / 1,4-dioxane; tetrahydrofuran / 3 h / 20 °C

With hydrogenchloride; potassium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; 1,2-dimethoxyethane; water;