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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743645Generated: October 31, 2026

Water → HCID 67732731, compound

https://huagongshe.com/reaction/743645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant7,8-Difluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acidHCID 11197026—
ReactantHCID 86749834HCID 86749834—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 67732731HCID 6773273178.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of 18 g of trans-3-amino-2-methylazetidine dimethanesulphonate and 12.7 g of triethylamine in 150 cm3 of dimethyl sulphoxide is heated with stirring to approximately 70° C. for 20 minutes. At the same temperature, 14.5 g of 7,8-difluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid are added in small portions in the course of 10 minutes, and the mixture is heated to approximately 90° C. for 2 hours. After cooling to approximately 20° C., the reaction mixture is poured into 400 cm3 of water at the same temperature. The insoluble matter is drained, washed with twice 100 cm3 of water and twice 100 cm3 of ethanol and recrystallized in 300 cm3 of dimethylformamide. 13.9 g of 8-(trans-3-amino-2-methyl-1-azetidinyl)-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid are obtained in the form of a yellow solid, which decomposes at 265°-267° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05556861
Source datasetuspto-grants-1996_09
ORD IDord-c22eded1065f4834a4ee220b839cbc68
Source noteuspto-grants-1996_09