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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 508071Erstellt: 26. Oktober 2026

Tributylphosphine → Tert-butyl 3-(4-{({2',6'-dimethyl-4'-[2-(2-oxopyrrolidin-1-yl)ethoxy]biphenyl-3-yl}methyl)[(2-nitrophenyl)sulfonyl]amino}-2-fluorophenyl)propanoate

https://huagongshe.com/reaction/508071

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTributylphosphineHCID 13831—
Edukt1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Edukt1-(2-Hydroxyethyl)-2-pyrrolidinoneHCID 76980—
EduktTert-butyl 3-(2-fluoro-4-{[(4'-hydroxy-2',6'-dimethylbiphenyl-3-yl)methyl][(2-nitrophenyl)sulfonyl]amino}phenyl)propanoateHCID 23157516—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktTert-butyl 3-(4-{({2',6'-dimethyl-4'-[2-(2-oxopyrrolidin-1-yl)ethoxy]biphenyl-3-yl}methyl)[(2-nitrophenyl)sulfonyl]amino}-2-fluorophenyl)propanoateHCID 2315746665%

Reaktionsschritte

To a solution of tert-butyl 3-(2-fluoro-4-{[(4′-hydroxy-2′,6′-dimethylbiphenyl-3-yl)methyl][(2-nitrophenyl)sulfonyl]amino}phenyl)propanoate (1.2 g, 1.89 mmol), 1-(2-hydroxyethyl)pyrrolidin-2-one (0.23 mL, 2.08 mmol) and tributylphosphine (0.75 mL, 2.84 mmol) in tetrahydrofuran (25 mL) was added 1,1′-(azodicarbonyl)dipiperidine (0.74 g, 2.84 mmol) under stirring at room temperature, and the mixture was stirred for 14 hr. The resulting precipitate was filtered off, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=10/1-ethyl acetate) to give the title compound (0.91 g, yield 65%) as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07786165B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-77f9a46160764b45988de1e658e42698
Quellennotizuspto-grants-2010_08