(1R,2R)-2-(tert-butyldimethylsilyloxy)-2-(3-chlorophenyl)-N-(cyclopropylmethyl)-1-(1-(phenylsulfonyl)-1H-indol-2-yl)ethanamine

Base Information

Chemical Name:(1R,2R)-2-(tert-butyldimethylsilyloxy)-2-(3-chlorophenyl)-N-(cyclopropylmethyl)-1-(1-(phenylsulfonyl)-1H-indol-2-yl)ethanamine
CAS No.:1429383-33-4
Molecular Formula:C₃₂H₃₉ClN₂O₃SSi
Molecular Weight:595.278
Hs Code.:

Synonyms:(1R,2R)-2-(tert-butyldimethylsilyloxy)-2-(3-chlorophenyl)-N-(cyclopropylmethyl)-1-(1-(phenylsulfonyl)-1H-indol-2-yl)ethanamine

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Chemical Property of (1R,2R)-2-(tert-butyldimethylsilyloxy)-2-(3-chlorophenyl)-N-(cyclopropylmethyl)-1-(1-(phenylsulfonyl)-1H-indol-2-yl)ethanamine

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Technology Process of (1R,2R)-2-(tert-butyldimethylsilyloxy)-2-(3-chlorophenyl)-N-(cyclopropylmethyl)-1-(1-(phenylsulfonyl)-1H-indol-2-yl)ethanamine

There total 10 articles about (1R,2R)-2-(tert-butyldimethylsilyloxy)-2-(3-chlorophenyl)-N-(cyclopropylmethyl)-1-(1-(phenylsulfonyl)-1H-indol-2-yl)ethanamine 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:

: 1429383-32-3
(1R,2R)-2-(tert-butyldimethylsilyloxy)-2-(3-chlorophenyl)-1-(1-(phenylsulfonyl)-1H-indol-2-yl)ethanamine

: 1489-69-6
Cyclopropanecarboxaldehyde

: 1429383-33-4
(1R,2R)-2-(tert-butyldimethylsilyloxy)-2-(3-chlorophenyl)-N-(cyclopropylmethyl)-1-(1-(phenylsulfonyl)-1H-indol-2-yl)ethanamine

Guidance literature:: (1R,2R)-2-(tert-butyldimethylsilyloxy)-2-(3-chlorophenyl)-1-(1-(phenylsulfonyl)-1H-indol-2-yl)ethanamine; Cyclopropanecarboxaldehyde; In methanol; at 20 ℃; for 1h;

With methanol; sodium tetrahydroborate; for 0.25h;

Reference yield:

: 40899-71-6
1-benzenesulfonylindole

: 1429383-33-4
(1R,2R)-2-(tert-butyldimethylsilyloxy)-2-(3-chlorophenyl)-N-(cyclopropylmethyl)-1-(1-(phenylsulfonyl)-1H-indol-2-yl)ethanamine

Guidance literature:: Multi-step reaction with 3 steps

1.1: n-butyllithium / tetrahydrofuran; hexane / 1.5 h / -78 - 0 °C / Inert atmosphere

1.2: 14 h / -78 - 20 °C / Inert atmosphere

2.1: hydrogenchloride / methanol; 1,4-dioxane / 0.75 h / 20 °C

3.1: methanol / 1 h / 20 °C

3.2: 0.25 h

With hydrogenchloride; n-butyllithium; In tetrahydrofuran; 1,4-dioxane; methanol; hexane;

Reference yield:

: 153294-02-1
(R)-2-(tert-butyldimethylsilyloxy)-2-(3-chlorophenyl)acetaldehyde

: 1429383-33-4
(1R,2R)-2-(tert-butyldimethylsilyloxy)-2-(3-chlorophenyl)-N-(cyclopropylmethyl)-1-(1-(phenylsulfonyl)-1H-indol-2-yl)ethanamine

Guidance literature:: Multi-step reaction with 4 steps

1.1: copper(II) sulfate / dichloromethane / 68 h / 20 °C

2.1: n-butyllithium / tetrahydrofuran; hexane / 1.5 h / -78 - 0 °C / Inert atmosphere

2.2: 14 h / -78 - 20 °C / Inert atmosphere

3.1: hydrogenchloride / methanol; 1,4-dioxane / 0.75 h / 20 °C

4.1: methanol / 1 h / 20 °C

4.2: 0.25 h

With hydrogenchloride; n-butyllithium; copper(II) sulfate; In tetrahydrofuran; 1,4-dioxane; methanol; hexane; dichloromethane;