Reaktion #157580

ord-4c7b0bbe0cd54786ac70ecd132d13340

Reaktionsgleichung

Nc1cc(Cl)ccc1S
2-amino-4-chloro-benzenethiol
Br.BrCc1cccnc1
3-bromomethyl-pyridine hydrobromide
O=S(=O)(Cl)c1cc2ccccc2o1
benzofuran-2-sulfonyl chloride
→
O=S(=O)(Nc1cc(Cl)ccc1SCc1cccnc1)c1cc2ccccc2o1
title compound
O=S(=O)(Nc1cc(Cl)ccc1SCc1cccnc1)c1cc2ccccc2o1
N-{5-chloro-2-[(pyridin-3-ylmethyl)thio]phenyl}-1-benzofuran-2-sulfonamide

Edukte

Nc1cc(Cl)ccc1S
2-amino-4-chloro-benzenethiol
Br.BrCc1cccnc1
3-bromomethyl-pyridine hydrobromide
O=S(=O)(Cl)c1cc2ccccc2o1
benzofuran-2-sulfonyl chloride

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

Following General Procedure A and B, the title compound was prepared from 2-amino-4-chloro-benzenethiol, 3-bromomethyl-pyridine hydrobromide, and benzofuran-2-sulfonyl chloride.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08822530B2uspto-grants-2014_09