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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256089Generated: October 30, 2026

Sodium Hydroxide → 8-Chloro-7-[3,7-diazabicyclo[3.3.0]oct-1(5)-ene-3-yl]-6-fluoro-1-[(1R,2S)-2-fluorocyclopropyl]-1,4-dihydro-4-oxoquinoline-3-carboxylic acid

https://huagongshe.com/reaction/2256089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant8-Chloro-6,7-difluoro-1-((1R,2S)-2-fluorocyclopropyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 10448547—
Reactant1,2,3,4,5,6-Hexahydropyrrolo[3,4-c]pyrrole dihydrobromideHCID 23282849—
SolventAcetonitrileHCID 6342—
Product8-Chloro-7-[3,7-diazabicyclo[3.3.0]oct-1(5)-ene-3-yl]-6-fluoro-1-[(1R,2S)-2-fluorocyclopropyl]-1,4-dihydro-4-oxoquinoline-3-carboxylic acidHCID 5436119210.7%

Reaction Steps

A solution of 318 mg of 8-chloro-6,7-difluoro-1-[(1R,2S)-2-fluorocyclopropyl]-1,4-dihydro-4-oxoquinoline-3-carboxylic acid, 544 mg of 3,7-diazabicyclo[3.3.0]oct-1(5) -ene dihydrobromide (JP-A-3-193779) and 2 ml of DBU in 20 ml of acetonitrile was heated under reflux for 15 hours. To the mixture was added 1N sodium hydroxide, and an insoluble material was removed by filtration. To the filtrate, was added hydrochloric acid till pH became 7.4, and the mixture was extracted by five 50 ml portions of chloroform. A combined organic layer was dried over anhydrous sodium sulfate and the solvent was removed under reduced pressure. The residue was recrystallized from a mixture of ethanol and ammonia water to yield 43.7 mg of the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05654318
Source datasetuspto-grants-1997_08
ORD IDord-182e778db8e14171b6fddad6184f080b
Source noteuspto-grants-1997_08