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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561156Generated: November 1, 2026

Ammonium Carbonate → Ethyl 6-amino-1-cyclopropyl-7-fluoro-1,4-dihydro-8-methoxy-5-nitro-4-oxoquinoline-3-carboxylate

https://huagongshe.com/reaction/561156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium CarbonateHCID 517111—
ReactantEthyl 1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-5-nitro-4-oxoquinoline-3-carboxylateHCID 10666701—
SolventDimethylformamideHCID 6228—
ProductEthyl 6-amino-1-cyclopropyl-7-fluoro-1,4-dihydro-8-methoxy-5-nitro-4-oxoquinoline-3-carboxylateHCID 5900295152%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of ethyl 1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methoxy-5-nitro-4-oxoquinoline-3-carboxylate (5.00 g, 13.5 mmol) and ammonium carbonate (11.7 g, 122 mmol) in DMF (50 mL) was stirred at 90° C. for 18 h. After the reaction mixture was poured into ice-water, the crude product was extracted with CH2Cl2, washed with brine, dried over MgSO4 and the solvent was removed in vacuo. The crude product washed with EtOH and dried to yield ethyl 6-amino-1-cyclopropyl-7-fluoro-1,4-dihydro-8-methoxy-5-nitro-4-oxoquinoline-3-carboxylate (2.55 g, 52%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063221B2
Source datasetuspto-grants-2011_11
ORD IDord-85f518514b554e1db6f8d527d3bec36a
Source noteuspto-grants-2011_11