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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 33439Erstellt: 24. Oktober 2026

Dimethylformamide → 6-Chloro-N-{(3S)-1-[(1S)-1-methyl-2-morpholin-4-yl-2-oxoethyl]-2-oxopyrrolidin-3-yl}-N-(2-morpholin-4-ylethyl)naphthalene-2-sulfonamide formate

https://huagongshe.com/de/reaction/33439

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktEthyl AcetateHCID 8857—
EduktPotassium CarbonateHCID 11430—
EduktMorpholine, 4-(2-chloroethyl)-, hydrochloride (1:1)HCID 77210—
Edukttert-Butyl(2R)-2-((3R)-3-{[(6-chloro-2-naphthyl)sulfonyl]amino}-2-oxopyrrolidin-1-yl)propanoateHCID 69222335—
LösungsmittelWaterHCID 962—
Produkt6-Chloro-N-{(3S)-1-[(1S)-1-methyl-2-morpholin-4-yl-2-oxoethyl]-2-oxopyrrolidin-3-yl}-N-(2-morpholin-4-ylethyl)naphthalene-2-sulfonamide formateHCID 10189365—

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

Example 1 (0.05 g) was dissolved in DMF (1 ml) and treated with chloroethylmorpholine hydrochloride (0.062 g) and potassium carbonate (0.093 g), and stirred at 40° C. for 2 h. The mixture was then heated at 80° C. for 8 h, cooled and treated with ethyl acetate and water. The organic extract was dried (over magnesium sulphate) and concentrated under reduced pressure. The residue was purified using mass directed preparative h.p.l.c. to give the title compound (0.018 g) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07429587B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-cfcdd9358193486a949f41d25c918519
Quellennotizuspto-grants-2008_09