HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylenediamine → 3,5-Diamino-N-(2-aminoethyl)-6-chloropyrazine-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Methyl 3,5-diamino-6-chloropyrazine-2-carboxylate | HCID 73827 | — |
| Product | 3,5-Diamino-N-(2-aminoethyl)-6-chloropyrazine-2-carboxamide | HCID 15148129 | 59% |
Reaction Steps
A mixture of 2.0 g (10.0 mmol) of methyl 3,5-diamino-6-chloropyrazine-2-carboxylate and 13.5 g (22.6 mmol) of ethylene diamine was allowed to stand for 3 days at ambient temperature. The excess amine was evaporated and the residue was crystallized from ethanol. There was obtained 1.38 g (5.9 mmol, 59%) of 3,5-diamino-6-chloro-N-(2-aminoethyl)pyrazine-2-carboxamide: mp 173°-174° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04906633 |
| Source dataset | uspto-grants-1990_03 |
| ORD ID | ord-8babb6f13acb491d84511385dbe76419 |
| Source note | uspto-grants-1990_03 |