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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277421Generated: October 30, 2026

2,6-Dihydroxyquinoline → HCID 13020228, compound

https://huagongshe.com/reaction/1277421

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DihydroxyquinolineHCID 177065—
ReactantHCID 54337875HCID 54337875—
SolventEthanolHCID 702—
ProductHCID 13020228HCID 13020228—

Reaction Steps

Into 100 ml of ethanol, 3.22 g of 6-hydroxycarbostyril and 3.51 ml of 1,5-diazabicyclo[5,4,0]-undecene-5 (DBU) are added and refluxed under stirring. Then 100 ml of ethanol containing 7 g of 1-benzyl-5-γ-iodopropyltetrazole is added dropwise for 90 minutes. After completion of the addition, the reaction mixture is further refluxedfor 5 hours and then concentrated. The residue is extracted with 300 ml of chloroform and the chloroform layer is washed with a diluted NaOH aqueous solution, a diluted hydrochloric acid and water and dried with Na2SO4. After the removal of the solvent, the residue is recrystallized from water-containing ethanol to obtain 4 g of 6-[3-(1-benzyltetrazol-5-yl)propoxy]carbostyril in the form of colorless needle-like crystals. Melting point: 152°-154° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04277479
Source datasetuspto-grants-1981_07
ORD IDord-6a9521382b4f492dbb47c27d33942e8b
Source noteuspto-grants-1981_07