HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Amino-6-methylpyrazine-2-carbonitrile → 4-Amino-2-ethoxymethyl-6-methylpteridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Amino-6-methylpyrazine-2-carbonitrile | HCID 584049 | — |
| Reactant | 2-Ethoxyethanimidamide | HCID 10725303 | — |
| Product | 4-Amino-2-ethoxymethyl-6-methylpteridine | HCID 10727593 | — |
Reaction Steps
A suspension of 15.1 g (0.113 mole) of 3-amino-6-methyl-2-pyrazinecarbonitrile [prepared according to E. C. Taylor et al., J. Am. Chem. Soc. 1973, 95, 6413] in the above ethanolic solution of 2-ethoxyacetamidine is refluxed for 2 hours. After cooling, the solution obtained is concentrated to dryness under reduced pressure. The residue is purified by washing with acetone and recrystallization from a mixture of acetone and isopropyl ether. Yld: 8.4 g (34%), m.p. 166°-168° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05167949 |
| Source dataset | uspto-grants-1992_12 |
| ORD ID | ord-ee4eebec7605483e952468842d8893b4 |
| Source note | uspto-grants-1992_12 |