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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant(5-Methyl-1H-imidazol-4-yl)(quinolin-7-yl)methanoneHCID 57965246—
SolventEthylene GlycolHCID 174—
Product7-((5-Methyl-1H-imidazol-4-yl)methyl)quinolineHCID 2499897865%

Reaction Conditions

Temperature120 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119807B2
Source datasetuspto-grants-2012_02
ORD IDord-2ac26afc246141d1a8f6e1cad364c62e
Source noteuspto-grants-2012_02