HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroformate → HCID 178473542, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | HCID 178513083 | HCID 178513083 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 178473542 | HCID 178473542 | — |
Reaction Steps
To a stirred suspension of N-amidino-3,5-diamino-6-chloro-2-pyrazinecarboxamide (27.6 g., 0.12 mole) in pyridine (300 ml.) is added ethyl chloroformate (12.0 ml., 0.15 mole) during a 5 minute period. The reaction is stirred at 25° for 2 hours during which time the starting material dissolves and the hydrochloride of the starting material precipitates. The latter is filtered from the reaction and discarded. The filtrate is treated with water (700 ml.) to give 16 g. (71%) of 3,5-diamino-6-chloro-N-[bis(ethoxycarbonylamino)methylene]-2-pyrazinecarboxamide which melts at 213° C. after recrystallization from ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04208413 |
| Source dataset | uspto-grants-1980_06 |
| ORD ID | ord-e04025a0269c4e9b920918f0016f0a49 |
| Source note | uspto-grants-1980_06 |