HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277421Generated: October 30, 2026
2,6-Dihydroxyquinoline → HCID 13020228, compound
https://huagongshe.com/reaction/1277421
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Dihydroxyquinoline | HCID 177065 | — |
| Reactant | HCID 54337875 | HCID 54337875 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13020228 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04277479 |
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| Source dataset | uspto-grants-1981_07 |
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| ORD ID | ord-6a9521382b4f492dbb47c27d33942e8b |
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| Source note | uspto-grants-1981_07 |
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