HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → N-(2,4-dimethoxybenzyl)-6-methoxyquinoxalin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2,4-Dimethoxybenzylamine | HCID 597250 | — |
| Reactant | 2-Chloro-6-methoxyquinoxaline | HCID 12686412 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | N-(2,4-dimethoxybenzyl)-6-methoxyquinoxalin-2-amine | HCID 57476556 | 94.1% |
Reaction Steps
2-Chloro-6-methoxyquinoxaline (0.93 g, 4.77 mmol) and (2,4-dimethoxyphenyl)methanamine (2.2 ml, 14.64 mmol) were microwaved in dimethylsulfoxide (5 mL) for 30 min at 150° C. The reaction was diluted into ethyl acetate (250 mL) and extracted with brine (3×100 mL). The crude product was purified by column chromatography (20 to 80% ethyl acetate/hexanes) to afford N-(2,4-dimethoxybenzyl)-6-methoxyquinoxalin-2-amine (1.46 g, 87% yield). 1H NMR (400 MHz, CDCl3) δ ppm 8.13 (1 H, s), 7.59-7.63 (1 H, m), 7.30 (1 H, d, J=8.31 Hz), 7.21-7.24 (2 H, m), 6.47 (1 H, d, J=2.27 Hz), 6.42 (1 H, dd, J=8.31, 2.27 Hz), 5.10 (1 H, t, J=5.92 Hz), 4.61 (2 H, d, J=5.79 Hz), 3.88 (3 H, s), 3.84 (3 H, s), 3.78 (3H, s). MS (LC/MS) R.T.=1.95; [M+H]+=326.23.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07863291B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-71ff177f30b04a63abe78681707e7b93 |
| Source note | uspto-grants-2011_01 |