2-[5-phenyl-4-(4-fluorobenzyl)-3-(3,4,5-trimethoxybenzoyl)-2-thienyl]-1H-isoindole-1,3(2H)-dione

Base Information

Chemical Name:2-[5-phenyl-4-(4-fluorobenzyl)-3-(3,4,5-trimethoxybenzoyl)-2-thienyl]-1H-isoindole-1,3(2H)-dione
CAS No.:1265049-13-5
Molecular Formula:C₃₅H₂₆FNO₆S
Molecular Weight:607.659
Hs Code.:

Synonyms:2-[5-phenyl-4-(4-fluorobenzyl)-3-(3,4,5-trimethoxybenzoyl)-2-thienyl]-1H-isoindole-1,3(2H)-dione

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Chemical Property of 2-[5-phenyl-4-(4-fluorobenzyl)-3-(3,4,5-trimethoxybenzoyl)-2-thienyl]-1H-isoindole-1,3(2H)-dione

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Technology Process of 2-[5-phenyl-4-(4-fluorobenzyl)-3-(3,4,5-trimethoxybenzoyl)-2-thienyl]-1H-isoindole-1,3(2H)-dione

There total 6 articles about 2-[5-phenyl-4-(4-fluorobenzyl)-3-(3,4,5-trimethoxybenzoyl)-2-thienyl]-1H-isoindole-1,3(2H)-dione 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: 62.0%

: 1265047-73-1
2-[4-bromomethyl-5-phenyl-3-(3,4,5-trimethoxybenzoyl)-2-thienyl]-1H-isoindole-1,3(2H)-dione

: 1765-93-1
4-fluoroboronic acid

: 1265049-13-5
2-[5-phenyl-4-(4-fluorobenzyl)-3-(3,4,5-trimethoxybenzoyl)-2-thienyl]-1H-isoindole-1,3(2H)-dione

Guidance literature:: With tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate; In toluene; at 120 ℃; for 18h; Inert atmosphere;
DOI:10.2174/157340610793563974

Reference yield:

: 901118-42-1
(2-amino-4-methylthiophen-3-yl)(3,4,5-trimethoxyphenyl)methanone

: 1265049-13-5
2-[5-phenyl-4-(4-fluorobenzyl)-3-(3,4,5-trimethoxybenzoyl)-2-thienyl]-1H-isoindole-1,3(2H)-dione

Guidance literature:: Multi-step reaction with 5 steps

1: acetic acid / 18 h / Reflux; Inert atmosphere

2: N-Bromosuccinimide; dibenzoyl peroxide / benzene / 6 h / Inert atmosphere; Reflux

3: tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate / toluene / 18 h / 120 °C / Inert atmosphere

4: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / 5 h / Inert atmosphere; Reflux

5: tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate / toluene / 18 h / 120 °C / Inert atmosphere

With N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate; acetic acid; dibenzoyl peroxide; In tetrachloromethane; toluene; benzene; 3: Suzuki coupling / 5: Suzuki coupling;
DOI:10.2174/157340610793563974

Reference yield:

: 901118-50-1
2-[4-methyl-3-(3,4,5-trimethoxybenzoyl)-2-thienyl]-1H-isoindole-1,3(2H)-dione

: 1265049-13-5
2-[5-phenyl-4-(4-fluorobenzyl)-3-(3,4,5-trimethoxybenzoyl)-2-thienyl]-1H-isoindole-1,3(2H)-dione

Guidance literature:: Multi-step reaction with 4 steps

1: N-Bromosuccinimide; dibenzoyl peroxide / benzene / 6 h / Inert atmosphere; Reflux

2: tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate / toluene / 18 h / 120 °C / Inert atmosphere

3: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / 5 h / Inert atmosphere; Reflux

4: tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate / toluene / 18 h / 120 °C / Inert atmosphere

With N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate; dibenzoyl peroxide; In tetrachloromethane; toluene; benzene; 2: Suzuki coupling / 4: Suzuki coupling;
DOI:10.2174/157340610793563974