N-[3-(3,6-dimethyl-4-oxo-4,5,6,7-tetrahydro-2H-isoindol-1-yl)-4-phenoxyphenyl]methanesulfonamide

Base Information

Chemical Name:N-[3-(3,6-dimethyl-4-oxo-4,5,6,7-tetrahydro-2H-isoindol-1-yl)-4-phenoxyphenyl]methanesulfonamide
CAS No.:1473453-17-6
Molecular Formula:C₂₃H₂₄N₂O₄S
Molecular Weight:424.521
Hs Code.:

Synonyms:N-[3-(3,6-dimethyl-4-oxo-4,5,6,7-tetrahydro-2H-isoindol-1-yl)-4-phenoxyphenyl]methanesulfonamide

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Chemical Property of N-[3-(3,6-dimethyl-4-oxo-4,5,6,7-tetrahydro-2H-isoindol-1-yl)-4-phenoxyphenyl]methanesulfonamide

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Technology Process of N-[3-(3,6-dimethyl-4-oxo-4,5,6,7-tetrahydro-2H-isoindol-1-yl)-4-phenoxyphenyl]methanesulfonamide

There total 5 articles about N-[3-(3,6-dimethyl-4-oxo-4,5,6,7-tetrahydro-2H-isoindol-1-yl)-4-phenoxyphenyl]methanesulfonamide 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:

: 1473453-15-4
1-(5-amino-2-phenoxyphenyl)-3,6-dimethyl-2,5,6,7-tetrahydro-4H-isoindol-4-one

: 124-63-0
methanesulfonyl chloride

: 1473453-17-6
N-[3-(3,6-dimethyl-4-oxo-4,5,6,7-tetrahydro-2H-isoindol-1-yl)-4-phenoxyphenyl]methanesulfonamide

Guidance literature:: 1-(5-amino-2-phenoxyphenyl)-3,6-dimethyl-2,5,6,7-tetrahydro-4H-isoindol-4-one; methanesulfonyl chloride; With triethylamine; In tetrahydrofuran; at 20 ℃; for 1.5h;

With sodium hydroxide; In tetrahydrofuran; water; at 45 ℃; for 1h;

Reference yield:

: 1473453-12-1
ethyl 3,6-dimethyl-4-oxo-4,5,6,7-tetrahydro-2H-isoindole-1-carboxylate

: 1473453-17-6
N-[3-(3,6-dimethyl-4-oxo-4,5,6,7-tetrahydro-2H-isoindol-1-yl)-4-phenoxyphenyl]methanesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: water; lithium hydroxide monohydrate / tetrahydrofuran / 72 h / 60 °C

1.2: 0.5 h / 100 °C

2.1: N-Bromosuccinimide / tetrahydrofuran / 0.5 h / -78 °C / Inert atmosphere

3.1: sodium carbonate; bis-triphenylphosphine-palladium(II) chloride / ethanol; 1,2-dimethoxyethane; water / 0.5 h / 20 - 120 °C / Microwave irradiation

4.1: triethylamine / tetrahydrofuran / 1.5 h / 20 °C

4.2: 1 h / 45 °C

With bis-triphenylphosphine-palladium(II) chloride; N-Bromosuccinimide; lithium hydroxide monohydrate; water; sodium carbonate; triethylamine; In tetrahydrofuran; 1,2-dimethoxyethane; ethanol; water; 3.1: |Suzuki Coupling;

Reference yield:

: 3,6-dimethyl-4-oxo-4,5,6,7-tetrahydro-2H-isoindole-1-carboxylic acid hydrogenchloride

: 1473453-17-6
N-[3-(3,6-dimethyl-4-oxo-4,5,6,7-tetrahydro-2H-isoindol-1-yl)-4-phenoxyphenyl]methanesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: N-Bromosuccinimide / tetrahydrofuran / 0.5 h / -78 °C / Inert atmosphere

2.1: sodium carbonate; bis-triphenylphosphine-palladium(II) chloride / ethanol; 1,2-dimethoxyethane; water / 0.5 h / 20 - 120 °C / Microwave irradiation

3.1: triethylamine / tetrahydrofuran / 1.5 h / 20 °C

3.2: 1 h / 45 °C

With bis-triphenylphosphine-palladium(II) chloride; N-Bromosuccinimide; sodium carbonate; triethylamine; In tetrahydrofuran; 1,2-dimethoxyethane; ethanol; water; 2.1: |Suzuki Coupling;