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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846700Generated: October 30, 2026

6,10-Dioxa-2-azaspiro[4.5]decane → 1-(2,4-Difluorophenyl)-7-(1,5-dioxa-8-azaspiro[5.4]dec-8-yl)-6-fluoro-1,8-naphthyridine-3-carboxylic acid

https://huagongshe.com/reaction/846700

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6,10-Dioxa-2-azaspiro[4.5]decaneHCID 19883338—
Reactant1-(2,4-Difluorophenyl)-7-chloro-6-fluoro-1,8-naphthyridine-3-carboxylic acid ethyl esterHCID 86746066—
Product1-(2,4-Difluorophenyl)-7-(1,5-dioxa-8-azaspiro[5.4]dec-8-yl)-6-fluoro-1,8-naphthyridine-3-carboxylic acidHCID 19883380—

Reaction Conditions

Temperature45 °C

Reaction Steps

Following the procedure of Step 2 Example 331 a 0.168 g (1.17 mmol) of 1,5-dioxa-8-azaspiro[5.4]decane, from Step 2 Example 14, was reacted with 0.300 g (0.78 mmol) of 1-(2,4-difluorophenyl)-7-chloro-6-fluoro-1,8-naphthyridine-3-carboxylic acid ethyl ester by heating at 40° C. instead of 45° C. for 10 instead of 24 hours. The solvent was removed by evaporation to afford the title product which was purified by column chromatography over silica gel (0% increasing to 4% methanol/methylene chloride) to afford 0.252 g of the title compound. The ester was not further purified, but was taken directly to the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05137892
Source datasetuspto-grants-1992_08
ORD IDord-52c9154fdfca406b8dc6ee68491ad955
Source noteuspto-grants-1992_08