tert-butyl (1-(4-(7-phenyl-2-(1H-pyrazol-4-yl)furo[2,3-b]pyrazin-6-yl)phenyl)cyclobutyl)carbamate

Base Information

Chemical Name:tert-butyl (1-(4-(7-phenyl-2-(1H-pyrazol-4-yl)furo[2,3-b]pyrazin-6-yl)phenyl)cyclobutyl)carbamate
CAS No.:1301612-85-0
Molecular Formula:C₃₀H₂₉N₅O₃
Molecular Weight:507.592
Hs Code.:

Synonyms:tert-butyl (1-(4-(7-phenyl-2-(1H-pyrazol-4-yl)furo[2,3-b]pyrazin-6-yl)phenyl)cyclobutyl)carbamate

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Chemical Property of tert-butyl (1-(4-(7-phenyl-2-(1H-pyrazol-4-yl)furo[2,3-b]pyrazin-6-yl)phenyl)cyclobutyl)carbamate

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Technology Process of tert-butyl (1-(4-(7-phenyl-2-(1H-pyrazol-4-yl)furo[2,3-b]pyrazin-6-yl)phenyl)cyclobutyl)carbamate

There total 6 articles about tert-butyl (1-(4-(7-phenyl-2-(1H-pyrazol-4-yl)furo[2,3-b]pyrazin-6-yl)phenyl)cyclobutyl)carbamate 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: 81.0%

: 269410-08-4
pyrazole-4-boronic acid pinacol ester

: 1301612-83-8
tert-butyl 1-(4-(2-chloro-7-phenylfuro[2,3-b]pyrazin-6-yl)phenyl)cyclobutylcarbamate

: 1301612-85-0
tert-butyl (1-(4-(7-phenyl-2-(1H-pyrazol-4-yl)furo[2,3-b]pyrazin-6-yl)phenyl)cyclobutyl)carbamate

Guidance literature:: With potassium phosphate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In water; N,N-dimethyl-formamide; at 20 - 120 ℃; for 0.333333h; Microwave irradiation; Inert atmosphere; Sealed tube;

Reference yield:

: 1032350-06-3
tert-butyl (1-(4-bromophenyl)cyclobutyl)carbamate

: 1301612-85-0
tert-butyl (1-(4-(7-phenyl-2-(1H-pyrazol-4-yl)furo[2,3-b]pyrazin-6-yl)phenyl)cyclobutyl)carbamate

Guidance literature:: Multi-step reaction with 6 steps

1: diisopropylamine / copper(l) iodide; bis(tri-t-butylphosphine)palladium⁽⁰⁾ / 1,4-dioxane / 20 h / 20 - 80 °C / Inert atmosphere

2: potassium carbonate; methanol / 1 h

3: triethylamine / copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide / 16 h / 80 °C / Inert atmosphere

4: iodine / dichloromethane / 0.25 h / 20 °C / Inert atmosphere

5: potassium phosphate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl-formamide; water / 16 h / 80 °C / Inert atmosphere

6: potassium phosphate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl-formamide; water / 0.33 h / 20 - 120 °C / Microwave irradiation; Inert atmosphere; Sealed tube

With methanol; potassium phosphate; iodine; potassium carbonate; triethylamine; diisopropylamine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; bis(tri-t-butylphosphine)palladium⁽⁰⁾; In 1,4-dioxane; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 1301610-33-2
tert-butyl 1-(4-ethynylphenyl)cyclobutylcarbamate

: 1301612-85-0
tert-butyl (1-(4-(7-phenyl-2-(1H-pyrazol-4-yl)furo[2,3-b]pyrazin-6-yl)phenyl)cyclobutyl)carbamate

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide / 16 h / 80 °C / Inert atmosphere

2: iodine / dichloromethane / 0.25 h / 20 °C / Inert atmosphere

3: potassium phosphate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl-formamide; water / 16 h / 80 °C / Inert atmosphere

4: potassium phosphate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / N,N-dimethyl-formamide; water / 0.33 h / 20 - 120 °C / Microwave irradiation; Inert atmosphere; Sealed tube

With potassium phosphate; iodine; triethylamine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In dichloromethane; water; N,N-dimethyl-formamide;