HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388191Generated: October 29, 2026
Oxygen → 2-(Benzo[d]thiazol-2-yl)quinolin-8-ol
https://huagongshe.com/reaction/388191
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxygen | HCID 977 | — |
| Reactant | 8-Hydroxyquinoline | HCID 1923 | — |
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | Phosphorus trichloride | HCID 24387 | — |
| Reactant | 8-Hydroxyquinaldic acid | HCID 74079 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(Benzo[d]thiazol-2-yl)quinolin-8-ol | HCID 136354101 | — |
Reaction Steps
To introduce a benzo[d]thiazol group into an 8-hydroxyquinoline compound, 2-aminothiophenol (123 mg, 1.1 mmol) and 8-hydroxyquinoline-2-carboxylic acid (189 mg, 2 mmol) were dissolved in dry toluene (30 ml) with blown nitrogen to prevent oxidation which is caused by oxygen in air. The solution was heated to 40° C. and phosphorus trichloride (0.1 ml, 1.1 mmol) was slowly added thereto. Then, the reaction solution was heated at 100° C. for 24 hours and allowed to cool. The reaction mixture was extracted with a 20% aqueous sodium carbonate solution, distilled water and dichloromethane, dried and recrystallized with dichloromethane and hexane to yield 2-(benzo[d]thiazol-2-yl)quinolin-8-ol, the compound of Formula 1 as a light green solid (yield: 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08377698B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-d4ab3e0f1b6c43559bd78b8005c6129b |
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| Source note | uspto-grants-2013_02 |
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