Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86757712 | HCID 86757712 | — |
| Solvent | Hydrochloride methanol | HCID 21893726 | — |
| Product | HCID 86757711 | HCID 86757711 | 99.9% |
Reaction Steps
(4aR, 12aR)-4a-(3-benzyloxyphenyl)-2-vinyloxycarbonyl-1,2,3,4,4a,5,12,12a-octahydroquinolino[2, 3-g]isoquinoline (181 mg, 0.369 mmol) was dissolved in a 10% hydrogen chloride methanol solution (6 ml), and the resultant solution was heated under reflux for 1 hour. After the solution was cooled to 0°C., an aqueous saturated sodiumbicarbonate solution (30 ml) and water (150 ml) were added to the solution, followed by extraction with chloroform (200 ml, 2 times). The organic layers were dried, and then concentrated to obtain the target compound (155 mg). The thus-obtained compound was supplied to next reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06337330B1 |
|---|
| Source dataset | uspto-grants-2002_01 |
|---|
| ORD ID | ord-f3dc1dafe36149a59d2beb17eff2eaa4 |
|---|
| Source note | uspto-grants-2002_01 |
|---|