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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031560Generated: November 1, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 14839609, compound

https://huagongshe.com/reaction/1031560

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 11844477HCID 11844477—
ReactantHCID 14839579HCID 14839579—
SolventAcetonitrileHCID 6342—
ProductHCID 14839609HCID 1483960922.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 653 mg (2 mmoles) 1-(1,1-dimethylethyl)-1,4-dihydro-6-fluoro-7-chloro-4-oxo-1,8-naphthyridine-3-carboxylic acid ethyl ester and 732 mg (3 mmoles) 8-trifluoroacetyl-3,8-diazabicyclo[3.2.1]octan,hydrochloride and 985 mg (6.48 mmoles) 1,8-diazabicyclo[5.4.0] undec-7-ene in 30 mL acetonitrile was heated at 60° C. for 72 hours. The solution was cooled and evaporated to dryness. The residue was worked up with dichloromethane and water. The organic layer was dried over magnesium sulfate and evaporated to give an oil. Purification was achieved by silicagel column chromatography to obtain 220 mg of 7-(8-trifluoroacetyl-3,8-diazabicyclo[3.2.1]octan-3-yl)-1-(1,1-dimethylethyl)-1,4-dihydro-6-fluoro-4-oxo-1,8-naphthyridine-3-carboxylic acid ethyl ester. MP 205° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04954507
Source datasetuspto-grants-1990_09
ORD IDord-0212bfd41a894116ba401ce6e88c703b
Source noteuspto-grants-1990_09