HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → Minoxidil
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 1-Acetoxy-6-amino-4-chloro-1,2-dihydro-2-iminopyrimidine | HCID 22164167 | — |
| Product | Minoxidil | HCID 4201 | 86% |
Reaction Steps
2.02 g (10 mmoles) of 1-acetoxy-6-amino-4-chloro-1,2-dihydro-2-iminopyrimidine are added to 8 ml of piperidine at room temperature while stirring. The mixture is stirred at room temperature for 2 hours, then piperidine is evaporated under reduced pressure. The residue is taken up in a mixture containing 20 ml of ethanol and 10 ml of 1N aqueous sodium hydroxide solution and refluxed for 30 minutes, then evaporated under reduced pressure. The residue is taken up in 20 ml of water, the crystals are filtered, washed with water and dried to give 1.74 g (86% yield) of the aimed compound which shows no melting point depression when mixed with the product of Example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04960888 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-5ccf13c07cc847a69a459dda945813ba |
| Source note | uspto-grants-1990_10 |