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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 40338Erstellt: 25. Oktober 2026

Dimethylacetamide → 6-(Difluoro(5-(3-methylisothiazol-5-yl)isoxazolo[4,5-b]pyridin-3-yl)methyl)quinoline

https://huagongshe.com/reaction/40338

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylacetamideHCID 31374—
Edukt5-Bromo-3-methylisothiazoleHCID 600959—
Edukt6-((5-Chloroisoxazolo[4,5-b]pyridin-3-yl)difluoromethyl)quinolineHCID 57690987—
EduktHCID 178461732HCID 178461732—
KatalysatorZincchlorideHCID 3007855—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
KatalysatorDitert-butyl(cyclopenta-2,4-dien-1-yl)phosphane;iron(2+);(2,3,4,5-tetraphenylcyclopenta-1,4-dien-1-yl)benzeneHCID 129828017—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt6-(Difluoro(5-(3-methylisothiazol-5-yl)isoxazolo[4,5-b]pyridin-3-yl)methyl)quinolineHCID 576910773,5%

Reaktionsbedingungen

Temperatur-40 °C

Reaktionsschritte

To a solution of 5-bromo-3-methylisothiazole (0.19 g, 1.1 mmol) in anhydrous THF (3 mL) was added isopropylmagnesium lithium chloride (1.0 M in THF, 1.5 mL, 1.5 mmol) at −40° C. The mixture was stirred at −40° C. for twenty minutes followed by the addition of zinc chloride (0.5 M in THF, 3.1 mL, 1.6 mmol). The mixture was brought to room temperature and stirred for thirty minutes followed by the addition of Q-Phos (0.12 g, 0.17 mmol), Pd2(dba)3 (0.097 g, 0.110 mmol), 6-((5-chloroisoxazolo[4,5-b]pyridin-3-yl)difluoromethyl)quinoline (0.10 g, 0.30 mmol), and anhydrous dimethylacetamide (3.5 mL). The mixture was stirred at 50° C. for ninety minutes then was diluted with ethyl acetate and washed with water. Organic extracts were dried over magnesium sulfate and purified by MPLC (eluted with a gradient of 10 to 50% ethyl acetate in hexanes), then purified by HPLC (eluted with a gradient of 15 to 90% acetonitrile in water) to afford the product as a white solid (4.2 mg, 3%). MS m/z=395.2 [M+1]+ Calc'd for C23H15F2N3O: 394.4.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524900B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-4519b5bad7b14b59aaf2797f1769ad78
Quellennotizuspto-grants-2013_09