HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Pyrazinecarboxylic acid → N-(2-aminoethyl)pyrazine-2-carboxamide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Pyrazinecarboxylic acid | HCID 1047 | — |
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Solvent | Ethyl chloroformate | HCID 10928 | — |
| Product | N-(2-aminoethyl)pyrazine-2-carboxamide hydrochloride | HCID 13800270 | — |
Reaction Steps
A solution of 25.0 g of pyrazinecarboxylic acid in 300 ml of methylene chloride and 20.1 ml of ethyl chloroformate was treated dropwise at 0° within 1/2 hour with 31 ml of triethylamine. After 1/2 hour the solution obtained was added dropwise at 0° to 68 ml of ethylenediamine in 200 ml of methylene chloride and the mixture was left to stir further for 1 hour without external cooling. Thereafter, the precipitated material was filtered off and the filtrate was evaporated to dryness on a rotary evaporator under reduced pressure. The residue was recrystallized twice from isopropanol, whereby there was obtained N-(2-aminoethyl)pyrazine-2-carboxamide hydrochloride, m.p. 205°-207°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04764522 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-30ebef72dd23407daacc55c956298292 |
| Source note | uspto-grants-1988_08 |