6-benzyloxy-7-methoxy-2-(3,4,5-trimethoxybenzoyl)-1,2,3,4-tetrahydroisoquinoline

Base Information

Chemical Name:6-benzyloxy-7-methoxy-2-(3,4,5-trimethoxybenzoyl)-1,2,3,4-tetrahydroisoquinoline
CAS No.:1064199-94-5
Molecular Formula:C₂₇H₂₉NO₆
Molecular Weight:463.53
Hs Code.:

Synonyms:6-benzyloxy-7-methoxy-2-(3,4,5-trimethoxybenzoyl)-1,2,3,4-tetrahydroisoquinoline

Suppliers and Price of 6-benzyloxy-7-methoxy-2-(3,4,5-trimethoxybenzoyl)-1,2,3,4-tetrahydroisoquinoline

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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-benzyloxy-7-methoxy-2-(3,4,5-trimethoxybenzoyl)-1,2,3,4-tetrahydroisoquinoline

Chemical Property:

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Technology Process of 6-benzyloxy-7-methoxy-2-(3,4,5-trimethoxybenzoyl)-1,2,3,4-tetrahydroisoquinoline

There total 11 articles about 6-benzyloxy-7-methoxy-2-(3,4,5-trimethoxybenzoyl)-1,2,3,4-tetrahydroisoquinoline 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: 79.0%

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

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

: 1064199-94-5
6-benzyloxy-7-methoxy-2-(3,4,5-trimethoxybenzoyl)-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: With triethylamine; In chloroform; at 20 ℃; for 18h;
DOI:10.1002/cmdc.201300261 DOI:10.1002/cmdc.201400017

Reference yield: 79.0%

: 1064199-94-5
6-benzyloxy-7-methoxy-2-(3,4,5-trimethoxybenzoyl)-1,2,3,4-tetrahydroisoquinoline

Guidance literature:

Reference yield:

: 36455-21-7
3-benzyloxy-4-methoxyphenylethylamine

: 1064199-94-5
6-benzyloxy-7-methoxy-2-(3,4,5-trimethoxybenzoyl)-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / dichloromethane / 4 h / 0 - 20 °C

2: toluene-4-sulfonic acid / toluene / 4 h / 120 °C

3: sodium hydroxide / water; ethanol / 16 h / 120 °C

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

With toluene-4-sulfonic acid; triethylamine; sodium hydroxide; In ethanol; dichloromethane; chloroform; water; toluene;
DOI:10.1002/cmdc.201300261