Reaktion #41995

ord-9ddee7899c3e41ddb990dad76578deab

Reaktionsgleichung

CCC1(c2c[nH]c3c(N)cccc23)CCc2cc(F)ccc21
3-(1-ethyl-5-fluoro-indan-1-yl)-1H-indol-7-ylamine
CCS(=O)(=O)Cl
ethanesulfonyl chloride
→
CCC1(c2c[nH]c3c(NS(=O)(=O)CC)cccc23)CCc2cc(F)ccc21
title compound
CCC1(c2c[nH]c3c(NS(=O)(=O)CC)cccc23)CCc2cc(F)ccc21
Ethanesulfonic acid [3-(1-ethyl-5-fluoro-indan-1-yl)-1H-indol-7-yl]-amide

Edukte

CCC1(c2c[nH]c3c(N)cccc23)CCc2cc(F)ccc21
3-(1-ethyl-5-fluoro-indan-1-yl)-1H-indol-7-ylamine
CCS(=O)(=O)Cl
ethanesulfonyl chloride

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

Utilizing 3-(1-ethyl-5-fluoro-indan-1-yl)-1H-indol-7-ylamine and ethanesulfonyl chloride, the title compound is prepared as in example 15. 0.18 g (35%). LC-MS m/z 387.1 (M++1).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07728150B2uspto-grants-2010_06