HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 178456790, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 178456767 | HCID 178456767 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178456790 | HCID 178456790 | 38.3% |
Reaction Steps
2 g of 2-amino-4-propylamino-6-chloropyrimidine 3-oxide, prepared according to the first two stages of the process of Example 1, are suspended in 20 ml of ethanol. 1.75 g of piperidine are added. The reaction mixture is refluxed for 19 hours. After it has returned to room temperature, 660 mg of potassium hydroxide are added as a solution in 10 ml of ethanol. After 1 hour's stirring the mixture is filtered on paper. The filtrates are evaporated to dryness. The residue is recrystallized from 25 ml of acetone. 950 mg of 2-amino-4-propylamino-6-piperidinopyrimidine 3-oxide are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05772990 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-5fb35e75ce8c4b839e15e63ac3bab436 |
| Source note | uspto-grants-1998_06 |