methyl 2-(6-(4-isobutyl-2-methoxybenzyloxy)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl)acetate

Base Information

Chemical Name:methyl 2-(6-(4-isobutyl-2-methoxybenzyloxy)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl)acetate
CAS No.:1262008-95-6
Molecular Formula:C₂₆H₃₂N₂O₄
Molecular Weight:436.551
Hs Code.:

Synonyms:methyl 2-(6-(4-isobutyl-2-methoxybenzyloxy)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl)acetate

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Chemical Property of methyl 2-(6-(4-isobutyl-2-methoxybenzyloxy)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl)acetate

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Technology Process of methyl 2-(6-(4-isobutyl-2-methoxybenzyloxy)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl)acetate

There total 5 articles about methyl 2-(6-(4-isobutyl-2-methoxybenzyloxy)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl)acetate 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:

: 1262008-94-5
2-(trimethylsilyl)ethyl 6-(4-isobutyl-2-methoxybenzyloxy)-1-(2-methoxy-2-oxoethyl)-3,4-dihydro-1H-pyrido[3,4-b]indole-2(9H)-carboxylate

: 1262008-95-6
methyl 2-(6-(4-isobutyl-2-methoxybenzyloxy)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl)acetate

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 24 ℃; for 19h;

Reference yield:

: 52055-23-9
5-benzyloxytryptamine hydrochloride

: 1262008-95-6
methyl 2-(6-(4-isobutyl-2-methoxybenzyloxy)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl)acetate

Guidance literature:: Multi-step reaction with 5 steps

1.1: trifluoroacetic acid; water / methanol / 80 °C

2.1: hydrogen / 10% palladium on activated charcoal / tetrahydrofuran; methanol / 1 h / 20 °C

3.1: chloro-trimethyl-silane; N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 24 °C

3.2: 18 h / 24 °C

3.3: 16 h / 24 °C

4.1: caesium carbonate / N,N-dimethyl-formamide / 0.17 h / 24 °C

4.2: 2 h / 50 °C

5.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 19 h / 24 °C

With chloro-trimethyl-silane; tetrabutyl ammonium fluoride; water; hydrogen; caesium carbonate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; 10% palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1262007-84-0
methyl 2-(6-(benzyloxy)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl)acetate

: 1262008-95-6
methyl 2-(6-(4-isobutyl-2-methoxybenzyloxy)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl)acetate

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydrogen / 10% palladium on activated charcoal / tetrahydrofuran; methanol / 1 h / 20 °C

2.1: chloro-trimethyl-silane; N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 24 °C

2.2: 18 h / 24 °C

2.3: 16 h / 24 °C

3.1: caesium carbonate / N,N-dimethyl-formamide / 0.17 h / 24 °C

3.2: 2 h / 50 °C

4.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 19 h / 24 °C

With chloro-trimethyl-silane; tetrabutyl ammonium fluoride; hydrogen; caesium carbonate; N-ethyl-N,N-diisopropylamine; 10% palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;