(R)-(1-methylpyrrolidin-2-yl)(5-(2-(phenylsulfonyl)ethyl)-1H-indol-3-yl)methanone

Base Information

Chemical Name:(R)-(1-methylpyrrolidin-2-yl)(5-(2-(phenylsulfonyl)ethyl)-1H-indol-3-yl)methanone
CAS No.:1027171-27-2
Molecular Formula:C₂₂H₂₄N₂O₃S
Molecular Weight:396.51
Hs Code.:

Synonyms:(R)-(1-methylpyrrolidin-2-yl)(5-(2-(phenylsulfonyl)ethyl)-1H-indol-3-yl)methanone

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Chemical Property of (R)-(1-methylpyrrolidin-2-yl)(5-(2-(phenylsulfonyl)ethyl)-1H-indol-3-yl)methanone

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Technology Process of (R)-(1-methylpyrrolidin-2-yl)(5-(2-(phenylsulfonyl)ethyl)-1H-indol-3-yl)methanone

There total 5 articles about (R)-(1-methylpyrrolidin-2-yl)(5-(2-(phenylsulfonyl)ethyl)-1H-indol-3-yl)methanone 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: 75.0%

: 50-00-0,30525-89-4,61233-19-0
formaldehyd

: 1225327-17-2
(R)-benzyl 2-(5-(2-(phenylsulfonyl)ethyl)-1H-indole-3-carbonyl)pyrrolidine-1-carboxylate

: 1027171-27-2
(R)-(1-methylpyrrolidin-2-yl)(5-(2-(phenylsulfonyl)ethyl)-1H-indol-3-yl)methanone

Guidance literature:: With methanesulfonic acid; hydrogen; palladium 10% on activated carbon; In acetone; under 2327.23 Torr;

Reference yield:

: (E)-5-(2-(phenylsulfonyl)vinyl)-1H-indole

: 1027171-27-2
(R)-(1-methylpyrrolidin-2-yl)(5-(2-(phenylsulfonyl)ethyl)-1H-indol-3-yl)methanone

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogen / palladium 10% on activated carbon / tetrahydrofuran; methanol / 2327.23 - 2585.81 Torr

2.1: ethylmagnesium bromide / dichloromethane; diethyl ether / 0.5 h / Reflux

2.2: 10 h / -25 - -15 °C

3.1: hydrogen; methanesulfonic acid / palladium 10% on activated carbon / acetone / 2327.23 Torr

With methanesulfonic acid; ethylmagnesium bromide; hydrogen; palladium 10% on activated carbon; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; acetone;

Reference yield:

: 10075-50-0
5-bromo-1H-indole

: 1027171-27-2
(R)-(1-methylpyrrolidin-2-yl)(5-(2-(phenylsulfonyl)ethyl)-1H-indol-3-yl)methanone

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine; tris-(o-tolyl)phosphine / palladium diacetate / N,N-dimethyl-formamide / 95 - 105 °C

2.1: hydrogen / palladium 10% on activated carbon / tetrahydrofuran; methanol / 2327.23 - 2585.81 Torr

3.1: ethylmagnesium bromide / dichloromethane; diethyl ether / 0.5 h / Reflux

3.2: 10 h / -25 - -15 °C

4.1: hydrogen; methanesulfonic acid / palladium 10% on activated carbon / acetone / 2327.23 Torr

With methanesulfonic acid; ethylmagnesium bromide; hydrogen; triethylamine; tris-(o-tolyl)phosphine; palladium 10% on activated carbon; palladium diacetate; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; N,N-dimethyl-formamide; acetone;