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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1742962Erstellt: 26. Oktober 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → (-)-9-Fluoro-3 (S)-methyl-10-[3-(1,2,3-triazol-1-yl) pyrrolidin-1-yl]-7-oxo-2,3-dihydro-7H-pyrido-[1,2,3de]-1,4-benzoxazine-6-carboxylic acid

https://huagongshe.com/reaction/1742962

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
EduktLevofloxacin q-acidHCID 688333—
Edukt1-(pyrrolidin-3-yl)-1H-1,2,3-triazole hydrochlorideHCID 19005943—
LösungsmittelAcetonitrileHCID 6342—
Produkt(-)-9-Fluoro-3 (S)-methyl-10-[3-(1,2,3-triazol-1-yl) pyrrolidin-1-yl]-7-oxo-2,3-dihydro-7H-pyrido-[1,2,3de]-1,4-benzoxazine-6-carboxylic acidHCID 702838599,3%

Reaktionsschritte

To a suspension of 76 mg (0.27 mmol) of (-) -9,10-difluoro-3(S)-methyl-7-oxo-2,3-dihydro-7H -pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid and 118 mg (0.675 mmol) of 3-(1,2,3-triazol-1-yl) pyrrolidine hydrochloride in 10 ml of dry acetonitrile was added 121 mg (0.81 mmol) of DBU. The reddish brown solution was refluxed for 31 hr. The solvent was then removed under reduced pressure. To the residue water was added and extracted with chloroform. The organic layer was then evaporated to dryness, and to the residue, water was added and solid collected to yield 10 mg of the desired product, m.p. 225°-229° C. 1H NMR (TFA) δ: 9.17 (s, 1H), 8.67 (s, 1H), 8.57 (s, 1H), 7.99 (d, 13.3Hz, 1H), 5.9-5.18 (m, 1H), 5.22-4.07 (m, 7H), 3.13-2.63 (m, 2H), 1.82 (s, 3H), 1.79 (s, 3H). Anal. calcd. for C19H18N5O4F . 1/2 H2O: C, 55.86; H, 4.69; N, 17.16. Found: C, 55.93; H, 4.59; N, 16.37.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05342846
Quelldatensatzuspto-grants-1994_08
ORD IDord-e2f2508567154e7e8b9bfdbae4d932bc
Quellennotizuspto-grants-1994_08