HuagongsheHuagongshe Chemistry Print Report · For research reference only
Amantadine → HCID 19428543, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Amantadine | HCID 2130 | — |
| Reactant | HCID 19428536 | HCID 19428536 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 19428543 | HCID 19428543 | — |
Reaction Steps
A solution of 26.0 g (87.25 mmoles) of 4,6-dichloro-2-(1-adamantylamino)pyrimidine and 39.5 g (261.6 mmoles) of 1-aminoadamantane in 200 ml of n-butanol, the reaction mixture is boiled under reflux for 24 hours, and evaporated. The residue is suspended in 400 ml of ether and filtered off. After drying, the filtered-off residue is purified by chromatography on a silica gel column and eluted with chloroform. After recrystallization from ether, the title compound is obtained in a yield of 23.94 g (66.44%), m.p.: 232°-236° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05547949 |
| Source dataset | uspto-grants-1996_08 |
| ORD ID | ord-0c93825290854db9af4d40871317748d |
| Source note | uspto-grants-1996_08 |