HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005686Generated: October 30, 2026
6-Ethoxycarbonylamino-1-methyl-3,4-dihydroisoquinoline → 6-Ethoxycarbonylamino-1-methylisoquinoline
https://huagongshe.com/reaction/1005686
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-Ethoxycarbonylamino-1-methyl-3,4-dihydroisoquinoline | HCID 22674119 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | P-Cymene | HCID 7463 | — |
| Product | 6-Ethoxycarbonylamino-1-methylisoquinoline | HCID 22674146 | 69% |
Reaction Steps
To 6-ethoxycarbonylamino-1-methyl-3,4-dihydroisoquinoline were added p-cymene (100 ml) and palladium-carbon (0.9 g), followed by heating under stirring at 195° C. in nitrogen atmosphere for 1 hour. After filtering off the catalyst, the reaction mixture was washed with ethanol and a part of the filtrate was evaporated. The residue was extracted with 1N hydrochloric acid, and then basified with potassium carbonate, followed by extracting with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate and the solvent was evaporated, to give the title compound (0.629 g, 69%, 2 steps) as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06787534B2 |
|---|
| Source dataset | uspto-grants-2004_09 |
|---|
| ORD ID | ord-cc620b2e56c34eaf9a16db20048571e6 |
|---|
| Source note | uspto-grants-2004_09 |
|---|