HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 19707385, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Phenylacetic Acid | HCID 999 | — |
| Reactant | Butylamine | HCID 8007 | — |
| Reactant | HCID 19707357 | HCID 19707357 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 19707385 | HCID 19707385 | — |
| Product | trans-4-n-Butyl-10b-methyl-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-3-one | HCID 53898870 | — |
Reaction Steps
By following the procedures described in Example 40, Steps A, B, C, D, E and F using phenylacetic acid as the starting material and in Step F using n-butylamine rather than ammonia and dimethoxyethane rather than ethylene glycol, the compound 4-n-butyl-10b-methyl-1,2,3,4,6,10b-hexahydrobenzo[f]quinolin-3-one was prepared. This hexahydrobenzo[f]quinolin-3-one was hydrogenated by following the procedures described Example 22 except that the reaction was carried out at 60° C. over 7 hours and worked up according to the procedures described in Example 42 to afford 61 mg of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05495021 |
| Source dataset | uspto-grants-1996_02 |
| ORD ID | ord-deb585822bed4c67800efaf62e721dec |
| Source note | uspto-grants-1996_02 |