(S)-1-[4-(allyloxy)benzyl]-5-[1-(2-methoxymethylpyrrolidinyl)sulfonyl]isatin

Base Information

Chemical Name:(S)-1-[4-(allyloxy)benzyl]-5-[1-(2-methoxymethylpyrrolidinyl)sulfonyl]isatin
CAS No.:1160524-35-5
Molecular Formula:C₂₄H₂₆N₂O₆S
Molecular Weight:470.546
Hs Code.:

Synonyms:(S)-1-[4-(allyloxy)benzyl]-5-[1-(2-methoxymethylpyrrolidinyl)sulfonyl]isatin

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Chemical Property of (S)-1-[4-(allyloxy)benzyl]-5-[1-(2-methoxymethylpyrrolidinyl)sulfonyl]isatin

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Technology Process of (S)-1-[4-(allyloxy)benzyl]-5-[1-(2-methoxymethylpyrrolidinyl)sulfonyl]isatin

There total 1 articles about (S)-1-[4-(allyloxy)benzyl]-5-[1-(2-methoxymethylpyrrolidinyl)sulfonyl]isatin 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:

: 143116-30-7
1-(allyloxy)-4-(bromomethyl)benzene

: 220509-74-0,1110670-49-9
(S)-5-[1-(2-methoxymethylpyrrolidinyl)sulfonyl]isatin

: 1160524-35-5
(S)-1-[4-(allyloxy)benzyl]-5-[1-(2-methoxymethylpyrrolidinyl)sulfonyl]isatin

Guidance literature:: (S)-5-[1-(2-methoxymethylpyrrolidinyl)sulfonyl]isatin; With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h; Inert atmosphere;

4-(prop-2-enyloxy)benzyl bromide; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 7.5h; Inert atmosphere;
DOI:10.1021/jm8015014

Reference yield:

: 1160524-35-5
(S)-1-[4-(allyloxy)benzyl]-5-[1-(2-methoxymethylpyrrolidinyl)sulfonyl]isatin

: 1160524-45-7
(S)-1-[4-(2-bromo-3-fluoropropoxy)benzyl]-5-[1-(2-methoxymethylpyrrolidinyl)sulfonyl]isatin

: 1160524-44-6
(S)-1-[4-(3-bromo-2-fluoropropoxy)benzyl]-5-[1-(2-methoxymethylpyrrolidinyl)sulfonyl]isatin

Guidance literature:: With N-Bromosuccinimide; pyridine hydrogenfluoride; In dichloromethane; at 0 - 20 ℃; for 6.5h; regioselective reaction; Inert atmosphere;
DOI:10.1021/jm8015014