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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651381Generated: November 3, 2026

1,3-Dichloro-2-propanol → Ethyl 1-cyclopropyl-6,8-difluoro-7-(3-hydroxy-1-azetidinyl)-1,4-dihydro-4-oxo-3-quinolinecarboxylate

https://huagongshe.com/reaction/1651381

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dichloro-2-propanolHCID 7289—
ReactantEthyl 7-amino-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylateHCID 10709913—
SolventPyridineHCID 1049—
ProductEthyl 1-cyclopropyl-6,8-difluoro-7-(3-hydroxy-1-azetidinyl)-1,4-dihydro-4-oxo-3-quinolinecarboxylateHCID 1561545355%

Reaction Steps

A solution of 0.8 g (2.60 mmoles) of ethyl 7-amino-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylate, 0.33 g (2.60 mmoles) of 1,3-dichloro-2-propanol and 25 ml of pyridine is agitated for 3 days, protected from light at ambient temperature; then left refluxing for 3 days and more. The solution is concentrated almost to dryness, poured onto water giving a precipitate which is filtered and washed with water. The solid is dried under vacuum, yielding 0.52 g (55%) of ethyl 1-cyclopropyl-6,8-difluoro-7-(3-hydroxy-1-azetidinyl)-1,4-dihydro-4-oxo-3-quinolinecarboxylate. Its melting point and spectroscopic data are identical to those of the derivative obtained according to method A.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04927926
Source datasetuspto-grants-1990_05
ORD IDord-dbf064aea1c14ceea09cd06236bde428
Source noteuspto-grants-1990_05