HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Methylpiperidine → HCID 178426353, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Methylpiperidine | HCID 79081 | — |
| Reactant | HCID 178522716 | HCID 178522716 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 178426353 | HCID 178426353 | — |
Reaction Steps
To a suspension of 1.13 g of 6-chloro-N-(1H-5-tetrazolyl)pyrazine-2-carboxamide in 20 ml of benzene, 2.94 ml of 3-methylpiperidine was added, and the mixture was refluxed for 6 hours. The reation mixture was evaporated, ethanol was added to the residue, and then the ethanol solution was adjusted with ethanolic hydrogen chloride to pH 3. The precipitate was collected by filtration, and recrystalized from a mixture of dimethylsulfoxide and methanol affording 0.81 g of the desired compound as pale yellow columns, m.p. 236.5°-238.5 ° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04792547 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-8d8ea68ecb5a4f2689781b9b3bb0b2fb |
| Source note | uspto-grants-1988_12 |