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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 8142Erstellt: 23. Oktober 2026

Tributylphosphine → (5S)-3-(3-fluoro-4-morpholino-phenyl)-5-[(isoxazol-3-ylamino)methyl]oxazolidin-2-one

https://huagongshe.com/de/reaction/8142

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTributylphosphineHCID 13831—
Edukt2,2,2-Trichloroethyl isoxazol-3-ylcarbamateHCID 1211419—
Eduktdiazenedicarboxylic acid bis(N,N-piperidide)HCID 5702657—
Edukt(5R)-3-(3-fluoro-4-morpholin-4-ylphenyl)-5-(hydroxymethyl)-1,3-oxazolidin-2-oneHCID 10541953—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(5S)-3-(3-fluoro-4-morpholino-phenyl)-5-[(isoxazol-3-ylamino)methyl]oxazolidin-2-oneHCID 497405331,2%

Reaktionsschritte

To a stirred solution of 3-(2,2,2-trichloroethyloxycarbonylamino)isoxazole (260 mg, 1.0 mmol), 5(R)-hydroxymethyl-3-(3-fluoro-4-morpholinophenyl)oxazolidin-2-one (see WO 95/07271; 293 mg, 1 mmol) and tributylphosphine (303 mg, 1.5 mmol) in dry tetrahydrofuran (10 ml) at 0° C. under a nitrogen atmosphere, was added 1,1-(azodicarbonyl)dipiperidine (378.5 mg, 1.5 mmol) in dry tetrahydrofuran (3 ml). The reaction allowed to warm to room temperature and was stirred for 4 days by which time a white suspension had formed. The reaction mixture was filtered and the residue washed with tetrahydrofuran. The filtrate was concentrated by rotary evaporation to give a yellow oil (1.2 g) which was purified by MPLC (30% ethyl acetate/hexane, ICN Alumina N 32–63) and further MPLC (100% CH2Cl2, ICN Alumina N 32–63). Concentration of the fractions by rotary evaporation gave the title compound as a crisp white foam (296 mg, 55%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087629B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-302209980d6547c5afc3a3106403db72
Quellennotizuspto-grants-2006_08