HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 89464205, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 6-methoxy-1-methyl-3,4-dihydroisoquinolin-7-ol | HCID 605698 | — |
| Reactant | Ethylbromopyruvate | HCID 21948992 | — |
| Product | HCID 89464205 | HCID 89464205 | — |
Reaction Steps
To a solution of 1-methyl-7-hydroxy-6-methoxy-3,4-dihydroisoquinoline (100 mg) in EtOH (5 ml) was added dropwise under a nitrogen atmosphere ethylbromopyruvate (0.065 ml) and the reaction mixture was heated under reflux for 2 hours. The reaction mixture was allowed to cool to ambient temperature, quenched with a saturated aqueous NaHCO3 solution and extracted with ethyl acetate. The organic layer was dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by chromatography on silica gel eluting with heptane and increasing amounts of ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09127007B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-008f0e764baf40209709184e4e89512e |
| Source note | uspto-grants-2015_09 |