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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600873Generated: October 30, 2026

Water → Ethyl 6-amino-7-fluoro-1-[2-(S)-fluoro-1-(R)-cyclopropyl]-1,4-dihydro-8-methoxy-5-nitro-4-oxoquinoline-3-carboxylate

https://huagongshe.com/reaction/600873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChloroformHCID 6212—
ReactantAzane;hydrateHCID 12896473—
ReactantEthyl 6,7-difluoro-1-[2-(S)-fluoro-1-(R)-cyclopropyl]-1,4-dihydro-8-methoxy-5-nitro-4-oxoquinoline-3-carboxylateHCID 67272160—
SolventDimethylformamideHCID 6228—
ProductEthyl 6-amino-7-fluoro-1-[2-(S)-fluoro-1-(R)-cyclopropyl]-1,4-dihydro-8-methoxy-5-nitro-4-oxoquinoline-3-carboxylateHCID 6727160364%

Reaction Steps

Ethyl 6,7-difluoro-1-[2-(S)-fluoro-1-(R)-cyclopropyl]-1,4-dihydro-8-methoxy-5-nitro-4-oxoquinoline-3-carboxylate (13.96 g, 36.14 mmol) was dissolved in dimethyl formamide (180 ml), and 28% ammonia water (60 ml) was added dropwise in while stirring and cooling with ice. After stirring the reaction solution at room temperature for 64 hours, water (100 ml) was added to the reaction solution and then concentrated under a reduced pressure. The water-containing residue obtained was then subjected to extraction with ethyl acetate (100 ml×3), and the organic layers were then combined, washed with water (150 ml×3) and saturated saline solution (200 ml) in that order, and then dried over anhydrous sodium sulfate. After filtering, the filtrate was concentrated under a reduced pressure, the residue obtained was applied to a silica gel chromatography, and 8.92 g (64%) of the title compound was obtained in the form of a pale red, oily substance from a chloroform:methanol=30:1 eluate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902226B2
Source datasetuspto-grants-2011_03
ORD IDord-6f23dd2f5bb44fc4be56f4bce738a77a
Source noteuspto-grants-2011_03