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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975334Generated: October 31, 2026

Tert-butyl 5-azaspiro[2.4]heptan-7-ylcarbamate → 7-(7-Tert-butoxycarbonylamino-5-azaspiro[2,4]heptan-5-yl)-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid

https://huagongshe.com/reaction/1975334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 5-azaspiro[2.4]heptan-7-ylcarbamateHCID 14930995—
Reactant1-Cyclopropyl-6,7-difluoro-2,3-dihydro-4-oxoquinoline-3-carboxylic acidHCID 15115582—
SolventDimethyl SulfoxideHCID 679—
Product7-(7-Tert-butoxycarbonylamino-5-azaspiro[2,4]heptan-5-yl)-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acidHCID 15338010—

Reaction Conditions

Temperature120 °C

Reaction Steps

250 mg of 1-cyclopropyl-6,7-difluoro-2,3-dihydro-4-oxoquinoline-3-carboxylic acid and 250 mg of compound 11 were added to 4 ml of dimethyl sulfoxide and the mixture was heated at 120° C. for 2 hours. After cooling, the solvent was removed under reduced pressure and the residue was crystallized by the addition of ethanol. The crystals were collected by filtration. The procedure gave 7-(7-tert-butoxycarbonylamino-5-azaspiro[2,4]heptan-5-yl)-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05286723
Source datasetuspto-grants-1994_02
ORD IDord-85a72b319b7e4891bcc6273c1e335d9e
Source noteuspto-grants-1994_02