6-benzyloxy-1-(3,5-diiodo-4-methoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

Base Information

Chemical Name:6-benzyloxy-1-(3,5-diiodo-4-methoxybenzyl)-1,2,3,4-tetrahydroisoquinoline
CAS No.:261913-78-4
Molecular Formula:C₂₄H₂₃I₂NO₂
Molecular Weight:611.261
Hs Code.:

Synonyms:6-benzyloxy-1-(3,5-diiodo-4-methoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

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Chemical Property of 6-benzyloxy-1-(3,5-diiodo-4-methoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

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Technology Process of 6-benzyloxy-1-(3,5-diiodo-4-methoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

There total 3 articles about 6-benzyloxy-1-(3,5-diiodo-4-methoxybenzyl)-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:

: 261913-76-2
N-(3-benzyloxyphenylethyl)-3,5-diiodo-4-methoxyphenylacetamide

: 261913-78-4
6-benzyloxy-1-(3,5-diiodo-4-methoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: N-(3-benzyloxyphenylethyl)-3,5-diiodo-4-methoxyphenylacetamide; With trichlorophosphate; In acetonitrile; for 4h; Heating;

With sodium tetrahydroborate; In methanol; at 20 ℃; Further stages.;
DOI:10.1021/jm990463j

Reference yield:

: 51061-22-4
2-(3-benzyloxyphenyl)ethylamine

: 261913-78-4
6-benzyloxy-1-(3,5-diiodo-4-methoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 2 steps

1.1: 86 percent / aq. NaOH / CH₂Cl₂ / 1.5 h

2.1: POCl₃ / acetonitrile / 4 h / Heating

2.2: NaBH₄ / methanol / 20 °C

With sodium hydroxide; trichlorophosphate; In dichloromethane; acetonitrile; 1.1: Acylation / 2.1: Cyclization / 2.2: Reduction;
DOI:10.1021/jm990463j

Reference yield:

: 221660-62-4
3,5-diiodo-4-methoxyphenylacetyl chloride

: 261913-78-4
6-benzyloxy-1-(3,5-diiodo-4-methoxybenzyl)-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 2 steps

1.1: 86 percent / aq. NaOH / CH₂Cl₂ / 1.5 h

2.1: POCl₃ / acetonitrile / 4 h / Heating

2.2: NaBH₄ / methanol / 20 °C

With sodium hydroxide; trichlorophosphate; In dichloromethane; acetonitrile; 1.1: Acylation / 2.1: Cyclization / 2.2: Reduction;
DOI:10.1021/jm990463j