HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 3-aminopyrazinecarboxylate → 3-(3-Oxo-butyrylamino)-pyrazine-2-carboxylic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 3-aminopyrazinecarboxylate | HCID 72669 | — |
| Reactant | 2,2,6-Trimethyl-4H-1,3-dioxin-4-one | HCID 79368 | — |
| Product | 3-(3-Oxo-butyrylamino)-pyrazine-2-carboxylic acid methyl ester | HCID 58114919 | — |
Reaction Steps
3-Aminopyrazine-2-carboxylic acid methyl ester (12 g) and 2,2,6-trimethyl-[1,3]dioxin-4-one (15.6 ml) were heated to reflux for 6 hours. The reaction mixture was concentrated. The residue was purified by column chromatography on silica gel (eluent: ethyl acetate/hexane 4:1, then ethyl acetate) to give 3-(3-oxo-butyrylamino)-pyrazine-2-carboxylic acid methyl ester as a beige solid (15 g). 1H-NMR (400 MHz, CDCl3): 2.33 (s, 3H), 3.91 (s, 2H), 4.05 (s, 3H), 8.40 (d, 1H), 8.51 (d, 1H), 10.06 (s, 1H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08653078B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-f18e11a35c154cef83d2e1cfeaec1130 |
| Source note | uspto-grants-2014_02 |