tert-butyl 3-(3-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)isoquinolin-1-yl)benzoate

Base Information

Chemical Name:tert-butyl 3-(3-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)isoquinolin-1-yl)benzoate
CAS No.:1152274-55-9
Molecular Formula:C₃₁H₂₆F₂N₂O₅
Molecular Weight:544.555
Hs Code.:

Synonyms:tert-butyl 3-(3-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)isoquinolin-1-yl)benzoate

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Chemical Property of tert-butyl 3-(3-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)isoquinolin-1-yl)benzoate

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Technology Process of tert-butyl 3-(3-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)isoquinolin-1-yl)benzoate

There total 9 articles about tert-butyl 3-(3-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)isoquinolin-1-yl)benzoate 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: 97.0%

: 220210-56-0
3-(tert-butoxycarbonyl)phenylboronic acid

: 1152274-51-5
N-(1-Bromoisoquinolin-3-yl)-1-(2,2-difluorobenzo-[d][1,3]dioxol-5-yl)cyclopropanecarboxamide

: 1152274-55-9
tert-butyl 3-(3-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)isoquinolin-1-yl)benzoate

Guidance literature:: With sodium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,2-dimethoxyethane; water; at 80 ℃;

Reference yield:

: 33070-32-5
5-bromo-2,2-difluoro-2H-1,3-benzodioxole

: 1152274-55-9
tert-butyl 3-(3-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)isoquinolin-1-yl)benzoate

Guidance literature:: Multi-step reaction with 9 steps

1.1: triethylamine / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / acetonitrile / 15 h / Heating / reflux

2.1: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 20 °C

2.2: 0 °C

3.1: thionyl chloride / dichloromethane / 0 - 20 °C

4.1: dimethyl sulfoxide / 20 °C

5.1: sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride / water / 70 °C

6.1: sodium hydroxide; water / 2.5 h / Heating / reflux

7.1: thionyl chloride / N,N-dimethyl-formamide / 2 h / 20 °C

8.1: triethylamine / dichloromethane / 18 h / 20 °C

9.1: sodium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,2-dimethoxyethane; water / 80 °C

With sodium hydroxide; lithium aluminium tetrahydride; thionyl chloride; N-benzyl-N,N,N-triethylammonium chloride; water; sodium carbonate; triethylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 68119-31-3
2-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)acetonitrile

: 1152274-55-9
tert-butyl 3-(3-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)isoquinolin-1-yl)benzoate

Guidance literature:: Multi-step reaction with 5 steps

1: sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride / water / 70 °C

2: sodium hydroxide; water / 2.5 h / Heating / reflux

3: thionyl chloride / N,N-dimethyl-formamide / 2 h / 20 °C

4: triethylamine / dichloromethane / 18 h / 20 °C

5: sodium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,2-dimethoxyethane; water / 80 °C

With sodium hydroxide; thionyl chloride; N-benzyl-N,N,N-triethylammonium chloride; water; sodium carbonate; triethylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,2-dimethoxyethane; dichloromethane; water; N,N-dimethyl-formamide;