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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716963Generated: October 31, 2026

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

https://huagongshe.com/reaction/716963

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 numberUS09193693B2
Source datasetuspto-grants-2015_11
ORD IDord-ad40045351c34b409d89f0062ab16053
Source noteuspto-grants-2015_11