HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 86583938, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Reactant | HCID 86583939 | HCID 86583939 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178526986 | HCID 178526986 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86583938 | HCID 86583938 | — |
Reaction Steps
A solution of 5.0 g (17.17 mmol) of 3,4-dihydro-3-(4-piperidinyl)-2(1H)-quinazolinone-acetate in 70 ml of methanol was hydrogenated at room temperature and in the presence of 1.0 g rhodium (III) oxide-platinum (IV) oxide hydrate catalyst (46.45% rhodium, 20.15% platinum) until the hydrogen uptake had ceased. The catalyst and solvent were removed, the residue was triturated with 10 ml of diisopropylether and a few drops of isopropanol and the resulting crystals were suction filtered. After drying in vacuo 4.4 g (86.2% of theory) of colourless crystals were obtained, Rf=0.3 (eluant: dichloromethane/methanol/conc. ammonia 7.5/2.5/0.5 v/v/v).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06344449B1 |
| Source dataset | uspto-grants-2002_02 |
| ORD ID | ord-3c885f785e9149908def7994e6e1748c |
| Source note | uspto-grants-2002_02 |