HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Aminopyrazine-2-carbonitrile → 2-(Ethoxymethyl)pteridin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Aminopyrazine-2-carbonitrile | HCID 817699 | — |
| Reactant | 2-Ethoxyethanimidamide | HCID 10725303 | — |
| Product | 2-(Ethoxymethyl)pteridin-4-amine | HCID 10798277 | — |
Reaction Steps
A mixture of 36.0 g (0.30 mole) of 3-amino-2-pyrazinecarbonitrile [prepared according to A. Albert and K. Ohta, J. Chem. Soc. C, 1970, 1540] and 46.7 g of 2-ethoxyacetamidine in 700 ml of absolute control is refluxed for 2 hours 30 minutes under a nitrogen atmosphere. After cooling, the precipitate obtained is isolated by filtration. It is purified by recrystallization from ethanol. Yld: 52.0 g (84%), m.p. 152°-154° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05167949 |
| Source dataset | uspto-grants-1992_12 |
| ORD ID | ord-6187666e7e50431bbe411d338d125dd0 |
| Source note | uspto-grants-1992_12 |