HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559566Generated: October 30, 2026
8-Hydroxyquinoline → HCID 178474185, compound
https://huagongshe.com/reaction/559566
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 8-Hydroxyquinoline | HCID 1923 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178474184 | HCID 178474184 | — |
| 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 178474185 | HCID 178474185 | 6.6% |
Reaction Steps
A mixture of (E)-N-(1-(4-iodophenyl)pyridin-2(1H)-ylidene)acetamide (120 mg, 0.27 mmol), 5-Chloro-N-((1H-imidazol-4-yl)methyl)thiophene-2-carboxamide 3-1 (109 mg, 0.30 mmol), 8-hydroxyquinoline (15 mg, 0.10 mmol) and K2CO3 (100 mg, 0.72 mmol) in DMSO (2 mL) was degassed with Ar before being charged with CuI (24 mg, 0.12 mmol). The mixture in a sealed tube was heated at 130° C. for 5 h. It was then purified by HPLC to give the titled compound (8 mg). MS 452.0 and 454.0 (M+H, Cl pattern).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08063077B2 |
|---|
| Source dataset | uspto-grants-2011_11 |
|---|
| ORD ID | ord-bdf89772379341ea98d7d66150557a7f |
|---|
| Source note | uspto-grants-2011_11 |
|---|