1,2,3,4-Tetrahydro-6-methoxy-2-(trifluoroacetyl)-1-[2-(3,4,5-trimethoxyphenyl)ethyl]-7-isoquinolinol

Base Information

Chemical Name:1,2,3,4-Tetrahydro-6-methoxy-2-(trifluoroacetyl)-1-[2-(3,4,5-trimethoxyphenyl)ethyl]-7-isoquinolinol
CAS No.:56771-99-4
Molecular Formula:C₂₃H₂₆F₃NO₆
Molecular Weight:469.458
Hs Code.:

Synonyms:1,2,3,4-Tetrahydro-6-methoxy-2-(trifluoroacetyl)-1-[2-(3,4,5-trimethoxyphenyl)ethyl]-7-isoquinolinol

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Chemical Property of 1,2,3,4-Tetrahydro-6-methoxy-2-(trifluoroacetyl)-1-[2-(3,4,5-trimethoxyphenyl)ethyl]-7-isoquinolinol

Chemical Property:

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Technology Process of 1,2,3,4-Tetrahydro-6-methoxy-2-(trifluoroacetyl)-1-[2-(3,4,5-trimethoxyphenyl)ethyl]-7-isoquinolinol

There total 7 articles about 1,2,3,4-Tetrahydro-6-methoxy-2-(trifluoroacetyl)-1-[2-(3,4,5-trimethoxyphenyl)ethyl]-7-isoquinolinol 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:

: 67393-36-6
N-trifluoroacetyl-7-benzyloxy-6-methoxy-1-(3',4',5'-trimethoxyphenethyl)-1,2,3,4-tetrahydroisoquinoline

: 56771-99-4,61659-91-4
N-trifluoroacetyl-7-hydroxy-6-methoxy-1-(3',4',5'-trimethoxyphenethyl)-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; for 3h; Inert atmosphere;
DOI:10.1016/j.bmcl.2012.04.007

Reference yield:

: 25173-72-2
3-(3,4,5-trimethoxyphenyl)propanoic acid

: 56771-99-4,61659-91-4
N-trifluoroacetyl-7-hydroxy-6-methoxy-1-(3',4',5'-trimethoxyphenethyl)-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 5 steps

1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 2 h / 20 °C / Inert atmosphere

2: trichlorophosphate / acetonitrile / 1 h / Inert atmosphere; Reflux

3: sodium tetrahydroborate / tetrahydrofuran; methanol / 1 h / 0 - 20 °C / Inert atmosphere

4: triethylamine / dichloromethane / 0 °C / Inert atmosphere

5: palladium 10% on activated carbon; hydrogen / methanol / 3 h / 20 °C / Inert atmosphere

With dmap; sodium tetrahydroborate; palladium 10% on activated carbon; hydrogen; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trichlorophosphate; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/j.bmcl.2012.04.007

Reference yield:

: 20947-59-5
N-(4-benzyloxy-3-methoxyphenethyl)-3-(3',4',5'-trimethoxyphenyl)propionamide

: 56771-99-4,61659-91-4
N-trifluoroacetyl-7-hydroxy-6-methoxy-1-(3',4',5'-trimethoxyphenethyl)-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 4 steps

1: trichlorophosphate / acetonitrile / 1 h / Inert atmosphere; Reflux

2: sodium tetrahydroborate / tetrahydrofuran; methanol / 1 h / 0 - 20 °C / Inert atmosphere

3: triethylamine / dichloromethane / 0 °C / Inert atmosphere

4: palladium 10% on activated carbon; hydrogen / methanol / 3 h / 20 °C / Inert atmosphere

With sodium tetrahydroborate; palladium 10% on activated carbon; hydrogen; triethylamine; trichlorophosphate; In tetrahydrofuran; methanol; dichloromethane; acetonitrile;
DOI:10.1016/j.bmcl.2012.04.007