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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872703Generated: November 3, 2026

HCID 13338332, compound → HCID 18687355, compound

https://huagongshe.com/reaction/1872703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13338332HCID 13338332—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 18687355HCID 18687355—

Reaction Steps

9-Amino-6-chloro-3-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine, prepared according to R. M. DeMarinis et al, J. Med. Chem., 1984, 27, 918, (0.190 g, 0.90 mmol) was dissolved in 10% acetic acid in methanol (50 ml) and 10% Pd/C (150 mg) added. The mixture was stirred at room temperature, under hydrogen/atmos pressure for 4h, then filtered through Kieselguhr and evaporated in vacuo. Residual material was taken up into dichloromethane and 5% NaHCO3 solution; the organic layer was washed with brine, dried (Na2SO4) and evaporated in vacuo to afford the title compound as a colourless oil (133 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06110934
Source datasetuspto-grants-2000_08
ORD IDord-7083a86823b44a008a0674ab7ad662e4
Source noteuspto-grants-2000_08