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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742984Generated: October 25, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 86748098, compound

https://huagongshe.com/reaction/1742984

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantLevofloxacin q-acidHCID 688333—
Reactant4-(1H-1,2,3-triazol-1-yl)piperidine hydrochlorideHCID 19006018—
SolventAcetonitrileHCID 6342—
ProductHCID 86748098HCID 86748098—

Reaction Steps

4-(1,2,3-triazol-1-yl)piperidine hydrochloride (100 mg) and DBU (80 mg) were added to a suspension of (-)-9,10-difluoro-3(S)-methyl-7-oxo-2,3-dihydro-7H-pyrido [1,2,3-de]-1,4-benzoxazine-6-carboxylic acid in acetonitrile (5 ml). The reaction mixture was refluxed for 48 hrs followed by stirring at room temperature for an additional 48 hrs. The reaction mixture was concentrated and the residue was diluted with water. The separated solid was filtered, washed with water and dried to yield 30 mg of desired product. m.p. 254°-255° C. (dec). 1H NMR (TFA) δ: 9.4 (s, 1H), 8.67 (s, 1H), 8.57 (s, 1H), 8.16 (d, 11.43Hz, 1H), 5.6-5.1 (m, 2H), 5.0-4.7 (m, 2H), 4.45-4.05 (m, 4H), 3.1-2.6 (m, 4H), 1.86 (d, 6.3Hz, 3H). Anal. calcd. for C 20 H20FN5O4 . H2O; C, 55.68; H, 5.14; N, 16.23.Found C, 55.88; H, 4.762; N, 15.92.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05342846
Source datasetuspto-grants-1994_08
ORD IDord-45cff9e0cb794ad08d8deb25bc396a95
Source noteuspto-grants-1994_08