HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499802Generated: October 30, 2026
8-Hydroxyquinoline → HCID 178482154, compound
https://huagongshe.com/reaction/499802
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 8-Hydroxyquinoline | HCID 1923 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178482153 | HCID 178482153 | — |
| Reactant | HCID 178523075 | HCID 178523075 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 178482154 | HCID 178482154 | 25.3% |
Reaction Steps
A mixture of (E)-N-(1-(4-iodophenyl)pyridin-2(1H)-ylidene)methanamine (59 mg, 0.14 mmol), 5-Chloro-N-((1H-imidazol-4-yl)methyl)thiophene-2-carboxamide 3-1 (63 mg, 0.18 mmol), 8-hydroxyquinoline (10 mg, 0.069 mmol) and K2CO3 (100 mg, 0.72 mmol) in DMSO (1 mL) was degassed with Ar before being charged with CuI (15 mg, 0.079 mmol). The mixture in a sealed tube was heated at 130° C. overnight. It was then purified by HPLC to give the titled compound (15 mg). MS 424.1 and 426.1 (M+H, Cl pattern).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07767697B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-c908c954e51a40cf80bf3180a5054677 |
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| Source note | uspto-grants-2010_08 |
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