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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405528Generated: November 1, 2026

Methyl iodide → 3-(Cyclopropyl(methyl)amino)-2-phenylquinoxaline-6-carboxylic acid

https://huagongshe.com/reaction/1405528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 3-(cyclopropylamino)-2-phenylquinoxaline-6-carboxylateHCID 67042136—
SolventTetrahydrofuranHCID 8028—
Product3-(Cyclopropyl(methyl)amino)-2-phenylquinoxaline-6-carboxylic acidHCID 50991023—

Reaction Steps

Into a 50-mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of methyl 3-(cyclopropylamino)-2-phenylquinoxaline-6-carboxylate (182.4 mg, 0.56 mmol, 1.00 equiv, 98%) in tetrahydrofuran (17 mL). Sodium hydride (274.5 mg, 11.44 mmol, 20.00 equiv) was added. The resulting solution was stirred for 1 h at room temperature. This was followed by the dropwise addition of CH3I (809.4 mg, 5.70 mmol, 10.00 equiv) with stirring at 0° C. The resulting solution was allowed to react, with stirring, overnight at room temperature. The resulting mixture was concentrated under vacuum and diluted with 10 ml of water. The pH value of the aqueous solution was adjusted to 3-4 with 1N hydrogen chloride. The resulting solid was collected by filtration and washed with water and methanol. This resulted in 66.5 mg (36%) of 3-(cyclopropyl(methyl)amino)-2-phenylquinoxaline-6-carboxylic acid as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916560B2
Source datasetuspto-grants-2014_12
ORD IDord-664ce7cbb7be410e9476d9250e92c1ff
Source noteuspto-grants-2014_12