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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Ethoxycarbonylamino-1-methyl-3,4-dihydroisoquinolineHCID 22674119—
CatalystHCID 178418390HCID 178418390—
SolventP-CymeneHCID 7463—
Product6-Ethoxycarbonylamino-1-methylisoquinolineHCID 2267414669%

Reaction Conditions

Temperature195 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787534B2
Source datasetuspto-grants-2004_09
ORD IDord-cc620b2e56c34eaf9a16db20048571e6
Source noteuspto-grants-2004_09