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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295730Generated: November 1, 2026

Pyridine → HCID 13116432, compound

https://huagongshe.com/reaction/2295730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantN-PiperidinoethanolHCID 18232—
Reactant8-chloro-7-fluoro-5-oxo-1,2-dihydro-5H-thiazolo(3,2-a)quinoline-4-carboxylic acidHCID 10470045—
ProductHCID 13116432HCID 13116432—

Reaction Steps

A mixture of 500 mg (1.67 mmol) of 8-chloro-7-fluoro-5-oxo-1,2-dihydro-5H-thiazolo(3,2-a)-quinoline-4-carboxylic acid and 1.09 grams (8.34 mmol) of N-(beta-hydroxyethyl)-piperidine was suspended in 20 ml of pyridine and the mixture was heated to reflux for thirty two hours. When the reaction was completed, the mixture was cooled to a room temperature, crystals separated out therefrom were collected by filtration, successively washed with pyridine, ethanol and ether, and recrystallized from dimethyl formamide to give the title compound as pale yellow powders. Yield 426.6 mg (65 percent). Melting point 256° to 256.5° C. Elementary analysis calculated as C18H20FN3O4S: C 54.95, H 5.12, N 10.68; Found: C 54.52, H 5.14, N 10.73.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04426381
Source datasetuspto-grants-1984_01
ORD IDord-c70ba637521f4d6894b515cfa00e7864
Source noteuspto-grants-1984_01