HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 9811366, compound → HCID 21994031, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 9811366 | HCID 9811366 | — |
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21994031 | HCID 21994031 | 90% |
Reaction Steps
To a solution of 2.91 g (6.95 mM) of N-[1-(3-phenylpropan-1-yl)piperidin-4-yl]-5-thia-1,8b-diazaacenaphthylene-4-carboxamide in ethanol (10 ml) was added 10 ml (40 mM) of 4N-HCl/methanol at room temperature and the mixture was stirred at room temperature for several minutes. After the solvent was distilled off under reduced pressure, ethanol and diethyl ether were added to the residue. The resulting crystals were collected by filtration and rinsed with ethanol and diethyl ether to provide 3.08 g (90%) of N-[1-(3-phenylpropan-1-yl)piperidin-4-yl]-5-thia-1,8b-diazaacenaphthylene-4-carboxamide dihydrochloride as orange-colored solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06235731B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-3baf310e6adc4dcfa61b8b2e75f1c448 |
| Source note | uspto-grants-2001_05 |