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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 542893Erstellt: 25. Oktober 2026

5-chloro-N-methylpyridin-2-amine → 1,1-bis(phenylsulphonyl)-2-[N-(5-chloropyrid-2-yl)-N-methylamino]ethene

https://huagongshe.com/reaction/542893

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-chloro-N-methylpyridin-2-amineHCID 3837024—
Edukt1,1-Bis(phenylsulphonyl)-2-ethoxyetheneHCID 12400938—
KatalysatorHydrochloric AcidHCID 313—
Katalysator1,5-Diazabicyclo(4.3.0)non-5-eneHCID 76349—
LösungsmittelTolueneHCID 1140—
Produkt1,1-bis(phenylsulphonyl)-2-[N-(5-chloropyrid-2-yl)-N-methylamino]etheneHCID 20207440—

Reaktionsschritte

A mixture of 5-chloro-2-(methylamino)pyridine (0.41 g), 2-ethoxy-1,1-bis(phenylsulphonyl)ethene and concentrated hydrochloric acid (1 drop) in toluene (20 ml) was heated at reflux for 4 hours and then the mixture was treated with 1,5-diazabicyclo[4.3.0]-non-5-ene (3 drops) and heated at reflux for 18 hours. The reaction mixture was cooled and concentrated in vacuo to give an oil which was triturated with ethanol to give a brown solid which was recrystallised from toluene to give 1,1-bis(phenylsulphonyl)-2-[N-(5-chloropyrid-2-yl)-N-methylamino]ethene (0.2 g), mp. 205°-206° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04659727
Quelldatensatzuspto-grants-1987_04
ORD IDord-b3a9fe616479454fa1f454e11bde5baa
Quellennotizuspto-grants-1987_04