(2-{2-[5-(trans-4-tert-butyl-cyclohexyloxy)-2,3-dihydro-indol-1-yl]-2-oxo-ethylamino}-ethyl)-phosphonic acid diethyl ester

Base Information

Chemical Name:(2-{2-[5-(trans-4-tert-butyl-cyclohexyloxy)-2,3-dihydro-indol-1-yl]-2-oxo-ethylamino}-ethyl)-phosphonic acid diethyl ester
CAS No.:1266116-47-5
Molecular Formula:C₂₆H₄₃N₂O₅P
Molecular Weight:494.612
Hs Code.:

Synonyms:(2-{2-[5-(trans-4-tert-butyl-cyclohexyloxy)-2,3-dihydro-indol-1-yl]-2-oxo-ethylamino}-ethyl)-phosphonic acid diethyl ester

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Chemical Property of (2-{2-[5-(trans-4-tert-butyl-cyclohexyloxy)-2,3-dihydro-indol-1-yl]-2-oxo-ethylamino}-ethyl)-phosphonic acid diethyl ester

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Technology Process of (2-{2-[5-(trans-4-tert-butyl-cyclohexyloxy)-2,3-dihydro-indol-1-yl]-2-oxo-ethylamino}-ethyl)-phosphonic acid diethyl ester

There total 7 articles about (2-{2-[5-(trans-4-tert-butyl-cyclohexyloxy)-2,3-dihydro-indol-1-yl]-2-oxo-ethylamino}-ethyl)-phosphonic acid diethyl ester 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: 25.0%

: diethyl (2-aminoethyl)phosphonate oxalic acid salt

: 1266116-46-4
1-[5-(trans-4-tert-butyl-cyclohexyloxy)-2,3-dihydro-indol-1-yl]-2-chloro-ethanone

: 1266116-47-5
(2-{2-[5-(trans-4-tert-butyl-cyclohexyloxy)-2,3-dihydro-indol-1-yl]-2-oxo-ethylamino}-ethyl)-phosphonic acid diethyl ester

Guidance literature:: With potassium carbonate; lithium bromide; In N,N-dimethyl-formamide; at 70 ℃;

Reference yield:

: 172078-33-0
2,3-Dihydro-1H-indol-5-ol

: 1266116-47-5
(2-{2-[5-(trans-4-tert-butyl-cyclohexyloxy)-2,3-dihydro-indol-1-yl]-2-oxo-ethylamino}-ethyl)-phosphonic acid diethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: sodium hydrogencarbonate / chloroform / 20 °C

2: caesium carbonate / butanone; tert-butyl alcohol / 100 °C / Sealed tube

3: hydrogenchloride / 1,4-dioxane; tetrahydrofuran / 48 h / 20 °C

4: triethylamine / dichloromethane / 4 h / 0 °C

5: potassium carbonate; lithium bromide / N,N-dimethyl-formamide / 70 °C

With hydrogenchloride; sodium hydrogencarbonate; potassium carbonate; caesium carbonate; triethylamine; lithium bromide; In tetrahydrofuran; 1,4-dioxane; dichloromethane; chloroform; N,N-dimethyl-formamide; butanone; tert-butyl alcohol;

Reference yield:

: 170147-76-9
tert-butyl 5-hydroxy-2,3-dihydroindole-1-carboxylate

: 1266116-47-5
(2-{2-[5-(trans-4-tert-butyl-cyclohexyloxy)-2,3-dihydro-indol-1-yl]-2-oxo-ethylamino}-ethyl)-phosphonic acid diethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: caesium carbonate / butanone; tert-butyl alcohol / 100 °C / Sealed tube

2: hydrogenchloride / 1,4-dioxane; tetrahydrofuran / 48 h / 20 °C

3: triethylamine / dichloromethane / 4 h / 0 °C

4: potassium carbonate; lithium bromide / N,N-dimethyl-formamide / 70 °C

With hydrogenchloride; potassium carbonate; caesium carbonate; triethylamine; lithium bromide; In tetrahydrofuran; 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide; butanone; tert-butyl alcohol;