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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 593286Erstellt: 25. Oktober 2026

1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) → [3-((4-(4-Fluoro-2-methoxyphenyl)pyridin-2-yl)amino)phenyl]-methanesulfonamide

https://huagongshe.com/reaction/593286

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Edukt(3-Aminophenyl)methanesulfonamideHCID 13266255—
Edukt2-Chloro-4-(4-fluoro-2-methoxyphenyl)pyridineHCID 58432609—
Eduktsodium 2-methylpropan-2-olateHCID 178418730—
LösungsmittelDimethylformamideHCID 6228—
Produkt[3-((4-(4-Fluoro-2-methoxyphenyl)pyridin-2-yl)amino)phenyl]-methanesulfonamideHCID 60172239—

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

Intermediate A2 (119 mg, 0.5 mmol), (3-aminophenyl)methanesulfonamide (112 mg, 0.6 mmol), NaOC(CH3)3 (67 mg, 0.7 mmol), PdCl2(CH3CN)2 (6.5 mg, 0.025 mmol, 5 mol %), and (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) [Xantphos] (23 mg, 0.04 mmol, 8 mol %) were dissolved in dry DMF (4 mL) and purged for 10 minutes with nitrogen. After heating at 110° C. for 18 hours the reaction mixture was filtered and the residue washed with toluene. The filtrate was concentrated under reduced pressure and purified by automated column chromatography (ISCO, gradient MeOH/DCM). The collected fractions which contained the title compound were further purified by preparative HPLC to yield 24 mg (12%) of G1 as an off-white solid. 1H NMR (300 MHz, d6-DMSO, 298K) δ 3.84 (s, 3H), 4.22 (s, 2H), 6.81-6.94 (m, 5H), 6.98 (s, 1H), 7.07 (dd, J=11.7 Hz, J=4.2 Hz, 1H), 7.26 (t, J=6.6 Hz, 1H), 7.39 (dd, J=6.9 Hz, J=6.0 Hz, 1H), 7.56-7.61 (m, 1H), 7.79 (d, J=7.5 Hz, 1H), 8.16 (d, J=6.0 Hz, 1H), 9.12 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09242937B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-c67929852bdb4a339566a7461158a5dd
Quellennotizuspto-grants-2016_01