HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → N-tert-butylpyrazine-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Isobutylene | HCID 8255 | — |
| Reactant | 2,3-Dicyanopyrazine | HCID 300514 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | N-tert-butylpyrazine-2-carboxamide | HCID 4462842 | — |
| Product | 3-cyano-N-tert-butyl-2-pyrazinecarboxamide | HCID 54209485 | — |
Reaction Steps
A compound having the formula (4) can be obtained as follows. The corresponding 2, 3-dicyano-pyrazine is reacted with tert-butyl alcohol or isobutylene in the presence of sulfuric acid to obtain the corresponding N-tert-butyl-2-pyrazinecarboxamide and/or 3-cyano-N-tert-butyl-2-pyrazinecarboxamide. Then, thus obtained corresponding N-tert-butyl-2-pyrazinecarboxamide and/or 3-cyano-N-tert-butyl-2-pyrazinecarboxamide are hydrolyzed under an alkaline condition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05734055 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-db920a7cf3b74cdbbcd3ab9ee72edff5 |
| Source note | uspto-grants-1998_03 |