HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → trans-7-Methoxy-4-(4-(4-phenylbenzoylamino)butyl)-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | trans-7-Methoxy-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinoline | HCID 13611558 | — |
| Reactant | 4-(4-Phenylbenzoylamino)butyraldehyde | HCID 21712565 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | trans-7-Methoxy-4-(4-(4-phenylbenzoylamino)butyl)-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinoline | HCID 54493650 | — |
Reaction Steps
Sodium triacetoxyborohydride 0.83 g, 3.9 mmol) was added to a stirred mixture of trans-7-methoxy-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinoline (D6a, 0.57 g, 2.6 mmol) and 4-(4-phenylbenzoylamino)butyraldehyde (0.77 g, 2.9 mmol) in dichloromethane (50 ml) at room temperature. After stirring for 6 h, the mixture was poured onto saturated aqueous K2CO3 (40 ml) and extracted with dichloromethane (3×20 ml). The combined organic extracts were washed with brine, dried (Na2SO4) and concentrated in vacuo to afford a white solid which was chromatographed on silica using 40-100% ethyl acetate/pentane as elution gradient. The title compound was obtained as a white solid (1.2 g, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06080752 |
| Source dataset | uspto-grants-2000_06 |
| ORD ID | ord-3a96c2b8e8a846ac8b4350abf212a84d |
| Source note | uspto-grants-2000_06 |