HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514596Generated: October 28, 2026
Iodide Ion → 1H-imidazo[4,5-c]quinolin-1-yl ether
https://huagongshe.com/reaction/514596
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodide Ion | HCID 30165 | — |
| Reactant | 1H-imidazo[4,5-c]quinolin-1-ol | HCID 66620860 | — |
| Product | 1H-imidazo[4,5-c]quinolin-1-yl ether | HCID 21898024 | — |
Reaction Steps
In step (3) of Reaction Scheme IV a 1H-imidazo[4,5-c]quinolin-1-yl alcohol of Formula XXXII is alkylated with an iodide of Formula XXXI to provide a 1H-imidazo[4,5-c]quinolin-1-yl ether of Formula XXXIII. The 1H-imidazo[4,5-c]quinolin-1-yl alcohol of Formula XXXII represents a subset of the compounds represented by Formula XXI in Reaction Scheme III. The compound of Formula XXXII can be prepared using the procedure described for the synthesis of the compound of Formula XXI in Reaction Scheme III. In step (3), the alcohol of Formula XXXII can be reacted with sodium hydride in a suitable solvent such as N,N-dimethylformamide to form an alkoxide. The iodide is added to the alkoxide solution at ambient temperature and then stirred at an elevated temperature (approximately 100° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09107958B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-13e1173e2eb24de8b59ed4e5730b6a78 |
|---|
| Source note | uspto-grants-2015_08 |
|---|