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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1180994Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1180994

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTributylphosphineHCID 13831—
Edukt3-FuranmethanolHCID 20449—
EduktDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Edukt6-Chloro-N-{(3S)-1-[(1S)-1-methyl-2-(4-morpholinyl)-2-oxo ethyl]-2-oxo-3-pyrrolidinyl}-2-naphthalenesulfonamideHCID 6852168—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt6-Chloro-N-(3-furylmethyl)-N-{(3S)-1-[(1S)-1-methyl-2-morpholin-4-yl-2-oxoethyl]-2-oxopyrrolidin-3-yl}naphthalene-2-sulfonamideHCID 10143807—

Reaktionsschritte

A solution of 6-chloro-N-{(3S)-1-[(1S)-1-methyl-2-morpholin-4-yl-2-oxoethyl]-2-oxopyrrolidin-3-yl}naphthalene-2-sulfonamide (0.015 g) in THF (0.5 ml) was treated with diisopropyl azodicarboxylate (0.01 ml), 3-furanmethanol (0.004 ml) and tri-n-butylphosphine (0.008 ml) and shaken at room temperature for 60 h. The mixture was concentrated under reduced pressure and the residue purified by mass directed preparative h.p.l.c. to give the title compound (0.015 g) as a colourless gum.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07282497B2
Quelldatensatzuspto-grants-2007_10
ORD IDord-ede1744dfe864ec287015b0b16ea2eef
Quellennotizuspto-grants-2007_10