6-hydroxy-7-methoxy-2-(3,4,5-trimethoxybenzoyl)-3,4-dihydroisoquinolin-1(2H)-one

Base Information

Chemical Name:6-hydroxy-7-methoxy-2-(3,4,5-trimethoxybenzoyl)-3,4-dihydroisoquinolin-1(2H)-one
CAS No.:1064200-63-0
Molecular Formula:C₂₀H₂₁NO₇
Molecular Weight:387.389
Hs Code.:

Synonyms:6-hydroxy-7-methoxy-2-(3,4,5-trimethoxybenzoyl)-3,4-dihydroisoquinolin-1(2H)-one

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 6-hydroxy-7-methoxy-2-(3,4,5-trimethoxybenzoyl)-3,4-dihydroisoquinolin-1(2H)-one

Chemical Property:

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Technology Process of 6-hydroxy-7-methoxy-2-(3,4,5-trimethoxybenzoyl)-3,4-dihydroisoquinolin-1(2H)-one

There total 4 articles about 6-hydroxy-7-methoxy-2-(3,4,5-trimethoxybenzoyl)-3,4-dihydroisoquinolin-1(2H)-one 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: 96.0%

: 1064200-45-8
6-benzyloxy-7-methoxy-2-(3,4,5-trimethoxybenzoyl)-3,4-dihydroisoquinolin-1(2H)-one

: 1064200-63-0
6-hydroxy-7-methoxy-2-(3,4,5-trimethoxybenzoyl)-3,4-dihydroisoquinolin-1(2H)-one

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In tetrahydrofuran; methanol; at 20 ℃; for 24h;
DOI:10.1002/cmdc.201400017

Reference yield:

: 98809-69-9
6-(Benzyloxy)-7-methoxy-1,2,3,4-tetrahydroisoquinoline

: 1064200-63-0
6-hydroxy-7-methoxy-2-(3,4,5-trimethoxybenzoyl)-3,4-dihydroisoquinolin-1(2H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / chloroform / 18 h / 20 °C

2: 18-crown-6 ether; potassium permanganate / dichloromethane / 16 h / 20 °C

3: hydrogen; palladium 10% on activated carbon / methanol; tetrahydrofuran / 24 h / 20 °C

With potassium permanganate; 18-crown-6 ether; palladium 10% on activated carbon; hydrogen; triethylamine; In tetrahydrofuran; methanol; dichloromethane; chloroform;
DOI:10.1002/cmdc.201400017

Reference yield:

: 4521-61-3
3,4,5-Trimethoxybenzoyl chloride

: 1064200-63-0
6-hydroxy-7-methoxy-2-(3,4,5-trimethoxybenzoyl)-3,4-dihydroisoquinolin-1(2H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / chloroform / 18 h / 20 °C

2: 18-crown-6 ether; potassium permanganate / dichloromethane / 16 h / 20 °C

3: hydrogen; palladium 10% on activated carbon / methanol; tetrahydrofuran / 24 h / 20 °C

With potassium permanganate; 18-crown-6 ether; palladium 10% on activated carbon; hydrogen; triethylamine; In tetrahydrofuran; methanol; dichloromethane; chloroform;
DOI:10.1002/cmdc.201400017