HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643392Generated: October 31, 2026
Hydrochloric Acid → 7-((5-Methyl-1H-imidazol-4-yl)methyl)quinoline
https://huagongshe.com/reaction/1643392
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | (5-Methyl-1H-imidazol-4-yl)(quinolin-7-yl)methanone | HCID 57965246 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Product | 7-((5-Methyl-1H-imidazol-4-yl)methyl)quinoline | HCID 24998978 | 65% |
Reaction Steps
A mixture of (9) (0.53 g, 2.23 mmol), potassium hydroxide (0.50 g, 8.91 mol), and hydrazine hydrate (0.45 mL, 14.4 mmol) in ethylene glycol was heated at 120° C. for 1 h, then kept at 165° C. overnight. The reaction mixture was cooled to room temperature and acidified with 2 M HCl (aq) to pH˜4. The aqueous layer was washed with chloroform/isoprpanol (3:1, 200 ml). The aqueous layer was basified to pH˜7, and extracted with chloroform/isopropanol (3:1, 200 mL). The pooled organic layers were dried over magnesium sulfate. The mixture was filtered, and the solvents were removed under vacuum. The residue was purified by chromatography on silica gel with 3% saturated ammonia methanol in dichloromethane to give 7-((5-methyl-1H-imidazol-4-yl)methyl)quinoline (10) as a yellow foam (0.32 mg, 1.45 mmol, 65% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08119807B2 |
|---|
| Source dataset | uspto-grants-2012_02 |
|---|
| ORD ID | ord-2ac26afc246141d1a8f6e1cad364c62e |
|---|
| Source note | uspto-grants-2012_02 |
|---|