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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651401Generated: November 1, 2026

Triethylamine → HCID 23051790, compound

https://huagongshe.com/reaction/1651401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Cyclopropyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic Acid Ethyl EsterHCID 535415—
ReactantN-(Azetidin-3-yl)-2,2,2-trifluoroacetamide--hydrogen chloride (1/1)HCID 19423639—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 23051790HCID 2305179022%

Reaction Steps

A mixture of 1 g (3.2 mmoles) of ethyl 1-cyclopropyl-6,7,8-trifluoro-4-oxo-1,4-dihydro-quinoline-3-carboxylate, 0.98 g (4.8 mmoles) of 3-trifluoroacetamidoazetidine hydrochloride and 2 ml of triethylamine is heated in 15 ml of dimethyl sulphoxide for 4 hours at 80°-5° C. It is diluted with water and extracted with chloroform. The organic phase is washed with water and evaporated yielding 0.31 g (22% of ethyl 1-cyclopropyl-6,8-difluoro-1,4-dihydro-7-(3-trifluoroacetamido-1-azetidinyl)-4-oxo-3-quinolinecarboxylate which is then hydrolysed by heating a mixture of 0.1 g (0.22 mmoles) of this ester with 5 ml of 1N sodium hydroxide and 5 ml of ethanol. The mixture is cooled, evaporated and acidified with acetic acid. Filtering and washing with water yields 70 mg (96%) of 1-cyclopropyl-6,8-difluoro-7-(3-amino-1-azetidinyl)-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, melting at 214°-6° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04927926
Source datasetuspto-grants-1990_05
ORD IDord-9fc0a95954c8475fa3dad6a8b919916d
Source noteuspto-grants-1990_05