Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 29544Erstellt: 24. Oktober 2026

Binap, (A+-)- → N-[4-Chloro-2-(6-methyl-pyridine-3-carbonyl)-phenyl]-4-(cis-2,6-dimethyl-morpholin-4-yl)-3-fluoro-benzenesulfonamide

https://huagongshe.com/de/reaction/29544

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBinap, (A+-)-HCID 634876—
Edukt2,6-Dimethylmorpholine, cis-HCID 641500—
EduktPotassium phosphate, tribasic, monohydrateHCID 22031701—
Edukt4-Bromo-N-[4-chloro-2-(6-methyl-pyridine-3-carbonyl)-phenyl]-3-fluoro-benzenesulfonamideHCID 59788573—
KatalysatorPalladiumHCID 23938—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-[4-Chloro-2-(6-methyl-pyridine-3-carbonyl)-phenyl]-4-(cis-2,6-dimethyl-morpholin-4-yl)-3-fluoro-benzenesulfonamideHCID 59788542—

Reaktionsschritte

The title compound was prepared according to the general procedure for the synthesis of heterocyclyl and heteroaryl substituted phenylsulfonyl derivatives previously described, using 4-Bromo-N-[4-chloro-2-(6-methyl-pyridine-3-carbonyl)-phenyl]-3-fluoro-benzenesulfonamide 0.2 g (0.4 mmol), potassium phosphate tribasic monohydrate 0.570 g (2.4 mmol), rac-2,2′-bis (diphenylphosphino)-1,1′-binaphthyl 0.077 g (0.12 mmol), cis-2,6-dimethyl-morpholine 0.23 g (2 mmol) and Pd (dba)3 0.057 g (0.06 mmol) in 2 ml DMF. HPLC purification gave yellow compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07420055B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-5bba3fa6d3cb45bfbb0167fa9013705c
Quellennotizuspto-grants-2008_09