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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461031Generated: October 25, 2026

Ethyl 1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-5-nitro-1,4-dihydro-4-oxoquinoline-3-carboxylate → HCID 15023844, compound

https://huagongshe.com/reaction/1461031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-5-nitro-1,4-dihydro-4-oxoquinoline-3-carboxylateHCID 15023843—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductHCID 15023844HCID 1502384464.3%

Reaction Steps

3.0 g (0.0074 moles) of ethyl 1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-5-nitro-1,4-dihydro-4-oxoquinoline-3-carboxylate [(XX), R1 =--OCHF2, R3' =NO2, R17 =C2H5, X=F] [prepared as described in step (e) above] were dissolved in 800 ml of acetic acid by heating. 0.75 g of 5% w/w palladium-on-carbon was then added to the solution, and the mixture was stirred at 70°-80° C. for 3 hours under a current of hydrogen. At the end of this time, the reaction mixture was filtered, and the filtrate was concentrated by evaporation under reduced pressure. The residue was washed with diethyl ether to give 1.78 g of ethyl 5-amino-1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate as a colorless powder, melting at 295°-296° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05073556
Source datasetuspto-grants-1991_12
ORD IDord-97fdaf82670947978f76b0908598b0c4
Source noteuspto-grants-1991_12