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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 3-(cyclopropylamino)-2-phenylquinoxaline-6-carboxylate | HCID 67042136 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(Cyclopropyl(methyl)amino)-2-phenylquinoxaline-6-carboxylic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193693B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-ad40045351c34b409d89f0062ab16053 |
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| Source note | uspto-grants-2015_11 |
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