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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2397560Generated: October 30, 2026

Piperidine → 5-Piperidinoacetyl-8-hydroxycarbostyril

https://huagongshe.com/reaction/2397560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant5-(Chloroacetyl)-8-hydroxy-2(1H)-quinolinoneHCID 13260299—
SolventBenzeneHCID 241—
Product5-Piperidinoacetyl-8-hydroxycarbostyrilHCID 13195278—

Reaction Steps

10 g of 5-chloroacetyl-8-hydroxycarbostyril (IV) prepared in Example 4 or 8 was suspended in 50 ml of benzene, and 10 ml of piperidine (III) was added to the suspension followed by allowing the mixture to react while heating under refluxing and stirring for 6 hours. The reaction mixture was filtered to recover the reaction product which was then washed with benzene and then with 50 ml of isopropanol. The resulting insoluble material was dissolved in 150 ml of a 2% aqueous hydrochloric acid. The solution was concentrated to dryness under reduced pressure and the resulting residue was recrystallized from ethanol to obtain 7.5 g of white amorphous 5-piperidinoacetyl-8-hydroxycarbostyril (II) hydrochloride 1/2 hydrate having a melting point of 239° - 241° C. (with decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04022776
Source datasetuspto-grants-1977_05
ORD IDord-57f8e8aebf624c8e98f3a11b1d50c355
Source noteuspto-grants-1977_05