HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Methoxybenzylamine → HCID 136115967, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Methoxybenzylamine | HCID 21156 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 86626396 | HCID 86626396 | — |
| Reactant | HCID 86626397 | HCID 86626397 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 136115967 | HCID 136115967 | 20% |
Reaction Steps
7-Bromo-1-(3-methoxybenzyl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one. Methyl 2-(3,5-dibromopyrazin-2-ylamino)acetate (0.58 g, 1.8 mmol), 3-methoxybenzylamine (227 μL, 1.8 mmol), diisopropylethylamine (1 mL), and dimethylsulfoxide (1 mL) were heated to 100° C. for 3 d under nitrogen. The reaction was extracted with ethyl acetate and water. The organic layer was dried with magnesium sulfate, filtered and concentrated. The residue was purified on silica gel column (0-100% ethyl acetate in hexanes) to give the title compound (124 mg, 20% yield) as a pink solid. MS (ESI) m/z 349.0 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07981893B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-b846d2c0a040452b9ddbd0acb41e7693 |
| Source note | uspto-grants-2011_07 |