HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831998Generated: October 29, 2026
2-(Aminomethyl)-5-methylpyrazine → HCID 54724183, compound
https://huagongshe.com/reaction/1831998
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(Aminomethyl)-5-methylpyrazine | HCID 2756496 | — |
| Reactant | 4-Hydroxy-6-methyl-2-pyrone | HCID 54675757 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 54724183 | HCID 54724183 | 63% |
Reaction Steps
A mixture of 4-hydroxy-6-methyl-2-pyrone (5.0 g, 0.04 mol) and 5-aminomethyl-2-methylpyrazine (5.0 g, 0.041 mol) in water (25.0 ml) was heated at 100° C. for 1 h under argon atmosphere. The reaction mixture was cooled, and filtered the yellow precipitate. It was washed with ethanol, and dried in vacuo to afford the title compound (5.8 g, 63%) as a pale yellow powder: 1H NMR (DMSO-d6/400 MHz) δ 10.43 (br, 1H), 8.38 (d, 2H, J=5.2 Hz), 5.77 (d, 1H, J=2.0 Hz), 5.58 (d, 1H, J=2.0 Hz), 4.92 (s, 2H), 2.24 (s, 3H), and 2.22 (s, 3H); ES MS m/z 232 (M+H) Step 2 3-Bromo-4-hydroxy-6-methyl-1-[(5-methylpyrazin-2-yl)methyl]pyridin-2(1H)-one
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07067540B2 |
|---|
| Source dataset | uspto-grants-2006_06 |
|---|
| ORD ID | ord-fc480d1fa55546e29aa708fd2364fddd |
|---|
| Source note | uspto-grants-2006_06 |
|---|