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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885860Generated: November 1, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 57047319, compound

https://huagongshe.com/reaction/1885860

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant1-Cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acidHCID 5210422—
ReactantHCID 57473425HCID 57473425—
ProductHCID 57047319HCID 57047319—

Reaction Steps

In a manner similar to that of Example 14, the title compound of Example 13 (0.80 g) was coupled to 1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxo-3-quinoline carboxylic acid in the presence of DBU and the product was subjected to catalytic hydrogenation to remove the benzyl group, yielding 0.16 g of the title compound as a solid, mp 268°-271° , [α]D20 -69.3°(DMSO). NMR data was the same as for the

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05147873
Source datasetuspto-grants-1992_09
ORD IDord-4b16e9a219ef4927be4c3f0c4a4f6383
Source noteuspto-grants-1992_09