HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxy-1-phenyl-1,2-dihydroquinolin-2-one → 2-Aminotetralin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxy-1-phenyl-1,2-dihydroquinolin-2-one | HCID 54676161 | — |
| Reactant | 1-Ethyl-4-hydroxyquinolin-2(1H)-one | HCID 54684641 | — |
| Reactant | 4-Hydroxy-N-methylcarbostyril | HCID 54686436 | — |
| Reactant | 1-Allyl-4-hydroxy-2-oxo-1,2-dihydroquinoline | HCID 54719647 | — |
| Product | 2-Aminotetralin | HCID 34677 | — |
Reaction Steps
Following the procedure of Example 91, but starting from 4-hydroxy-1-methylcarbostyril, 4-hydroxy-1-ethylcarbostyril, 4-hydroxy-1-allylcarbostyril, or 4-hydroxy-1-phenylcarbostyril and reacting the raw chlorohydrin thus obtained with 2-aminotetralin, the following compounds are prepared respectively:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05254595 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-610acb47c1eb41b7bf192c49552853ce |
| Source note | uspto-grants-1993_10 |