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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2208899Generated: November 1, 2026

HCID 86719568, compound → HCID 70874407, compound

https://huagongshe.com/reaction/2208899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86719568HCID 86719568—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 70874407HCID 7087440720%

Reaction Steps

To a stirred solution of 3-(allyl(tetrahydro-2H-pyran-4-yl)amino)-5-chloro-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-2-methylbenzamide (0.10 g) in MeOH (10 mL) was added 10% Pd/C (0.03 g) and the reaction stirred at room temperature under hydrogen (balloon pressure) for 2 h. On completion, the reaction mixture was filtered through celite and the filtrate was concentrated under reduced pressure to obtain crude solid which was purified by column chromatography to afford the title compound (0.02 g, 20%). LCMS: 445.25 (M+1)+; HPLC: 90.40% (@ 254 nm) (Rt; 5.609; Method: Column: YMC ODS-A 150 mm×4.6 mm×5μ; Mobile Phase: A; 0.05% TFA in water/B; 0.05% TFA in acetonitrile; Inj. Vol: 10 μL, Col. Temp.: 30° C.; Flow rate: 1.4 mL/min.; Gradient: 5% B to 95% B in 8 min, Hold for 1.5 min, 9.51-12 min 5% B); 1H NMR (DMSO-d6, 400 MHz) δ 11.47 (s, 1H), 8.23 (t, 1H), 7.19 (s, 1H), 6.93 (d, 1H, J=1.6 Hz), 5.88 (s, 1H), 4.24 (d, 2H, J=4.4 Hz), 3.83 (d, 2H, J=10.4 Hz), 3.22-3.25 (m, 2H), 2.94 (t, 2H, J=7.2 Hz), 2.88-2.90 (m, 1H), 2.18 (s, 3H), 2.15 (s, 3H), 2.10 (s, 3H), 1.56 (m, 4H), 1.14-1.23 (m, 2H), 0.75 (t, 3H, J=8 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376422B2
Source datasetuspto-grants-2016_06
ORD IDord-dca4082ae9d540429680b6faadf7a840
Source noteuspto-grants-2016_06