HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716995Generated: October 27, 2026
Methyl iodide → (R)-3-(sec-Butyl(methyl)amino)-2-phenylquinoxaline-6-carboxylic acid
https://huagongshe.com/reaction/716995
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (R)-methyl 3-(sec-butylamino)-2-phenylquinoxaline-6-carboxylate | HCID 67042005 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (R)-3-(sec-Butyl(methyl)amino)-2-phenylquinoxaline-6-carboxylic acid | HCID 50991211 | — |
Reaction Steps
Into a 50-mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of (R)-methyl 3-(sec-butylamino)-2-phenylquinoxaline-6-carboxylate (110 mg, 0.33 mmol, 1.00 equiv) in tetrahydrofuran (9 mL). sodium hydride (132 mg, 3.3 mmol, 10.00 equiv, 60%) was added. The resulting solution was stirred for 1 h at room temperature. This was followed by the dropwise addition of a solution of CH3I (922.5 mg, 6.50 mmol, 20.00 equiv) in tetrahydrofuran (2 mL) with stiffing at 0° C. The resulting solution was stirred for overnight at 20° C. The resulting mixture was concentrated under vacuum and diluted by 10 ml of H2O. The pH value of the aqueous solution was adjusted to 3-4 with 1N hydrogen chloride. The resulting solid was collected by filtration. This resulted solid in 67 mg (59%) of (R)-3-(sec-butyl(methyl)amino)-2-phenylquinoxaline-6-carboxylic acid as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09193693B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-c8db8670991d450fb81a14543dd28195 |
|---|
| Source note | uspto-grants-2015_11 |
|---|