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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508974Generated: October 30, 2026

HCID 118036935, compound → HCID 118037283, compound

https://huagongshe.com/reaction/1508974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 118036935HCID 118036935—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 118037283HCID 11803728397.8%

Reaction Steps

To a solution of 2-(4-((2-(cyclopent-1-en-1-yl)-6,7-dihydro-5H-cyclopenta[b]pyridin-4-yl)amino)phenyl)acetamide hydrochloride (0.042 g, 0.11 mmol) in ethanol (10 mL) was added 10% palladium on carbon (0.005 g). The mixture stirred at rt for 2 h under an atmosphere of hydrogen. After this time, the mixture was filtered over celite, concentrated, and the residue converted to the hydrochloride salt to afford the title compound (0.040 g, 95%) as a white solid. MW=420.38. 1H NMR (DMSO-d6, 500 MHz) δ 13.60 (s, 1H), 9.59 (s, 1H), 7.52 (s, 1H), 7.36 (d, J=8.0 Hz, 1H), 7.26 (d, J=8.0 Hz, 2H), 6.92 (s, 1H), 6.69-6.66 (m, 1H), 3.42 (s, 1H), 3.18-3.04 (m, 3H), 2.83 (t, J=7.5 Hz, 2H), 2.18 (quin, J=7.5 Hz, 2H), 2.07-1.96 (m, 2H), 1.77-1.69 (m, 2H), 1.68-1.52 (m, 4H), 1.37-1.22 (m, 2H); APCI MS m/z 384 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221843B2
Source datasetuspto-grants-2015_12
ORD IDord-a419d11dcdac4e2b8a0ddf61b69c8265
Source noteuspto-grants-2015_12