tert-butyl 6-(2,4-bis(trifluoromethyl)benzyloxy)-1-(2-methoxy-2-oxoethyl)-3,4-dihydro-1H-pyrido[3,4-b]indole-2(9H)-carboxylate

Base Information

Chemical Name:tert-butyl 6-(2,4-bis(trifluoromethyl)benzyloxy)-1-(2-methoxy-2-oxoethyl)-3,4-dihydro-1H-pyrido[3,4-b]indole-2(9H)-carboxylate
CAS No.:1262008-16-1
Molecular Formula:C₂₈H₂₈F₆N₂O₅
Molecular Weight:586.531
Hs Code.:

Synonyms:tert-butyl 6-(2,4-bis(trifluoromethyl)benzyloxy)-1-(2-methoxy-2-oxoethyl)-3,4-dihydro-1H-pyrido[3,4-b]indole-2(9H)-carboxylate

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Chemical Property of tert-butyl 6-(2,4-bis(trifluoromethyl)benzyloxy)-1-(2-methoxy-2-oxoethyl)-3,4-dihydro-1H-pyrido[3,4-b]indole-2(9H)-carboxylate

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Technology Process of tert-butyl 6-(2,4-bis(trifluoromethyl)benzyloxy)-1-(2-methoxy-2-oxoethyl)-3,4-dihydro-1H-pyrido[3,4-b]indole-2(9H)-carboxylate

There total 5 articles about tert-butyl 6-(2,4-bis(trifluoromethyl)benzyloxy)-1-(2-methoxy-2-oxoethyl)-3,4-dihydro-1H-pyrido[3,4-b]indole-2(9H)-carboxylate 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:

: 1262007-89-5
tert-butyl 6-hydroxy-1-(2-methoxy-2-oxoethyl)-3,4-dihydro-1H-pyrido[3,4-b]indole-2(9H)-carboxylate

: 140690-56-8
2,4-bis(trifluoromethyl)benzyl bromide

: 1262008-16-1
tert-butyl 6-(2,4-bis(trifluoromethyl)benzyloxy)-1-(2-methoxy-2-oxoethyl)-3,4-dihydro-1H-pyrido[3,4-b]indole-2(9H)-carboxylate

Guidance literature:: With caesium carbonate; In N,N-dimethyl-formamide; at 20 ℃;

Reference yield:

: 52055-23-9
5-benzyloxytryptamine hydrochloride

: 1262008-16-1
tert-butyl 6-(2,4-bis(trifluoromethyl)benzyloxy)-1-(2-methoxy-2-oxoethyl)-3,4-dihydro-1H-pyrido[3,4-b]indole-2(9H)-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

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

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

3: triethylamine / 1,4-dioxane / 2 h / 20 °C

4: caesium carbonate / N,N-dimethyl-formamide / 20 °C

With water; hydrogen; caesium carbonate; triethylamine; trifluoroacetic acid; 10% palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; methanol; 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

: 1262008-16-1
tert-butyl 6-(2,4-bis(trifluoromethyl)benzyloxy)-1-(2-methoxy-2-oxoethyl)-3,4-dihydro-1H-pyrido[3,4-b]indole-2(9H)-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

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

2: triethylamine / 1,4-dioxane / 2 h / 20 °C

3: caesium carbonate / N,N-dimethyl-formamide / 20 °C

With hydrogen; caesium carbonate; triethylamine; 10% palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; methanol; N,N-dimethyl-formamide;