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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887488Generated: October 29, 2026

HCID 59351234, compound → HCID 59351206, compound

https://huagongshe.com/reaction/887488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59351234HCID 59351234—
CatalystPalladiumHCID 23938—
SolventDioxan ethanolHCID 22560076—
ProductHCID 59351206HCID 5935120638.1%

Reaction Steps

A solution of 4-(3-(4-(1H-benzo[d]imidazole-2-carbonyl)phenoxy)pyrazin-2-yl)-1-methyl-5,6-dihydropyridin-2(1H)-one (0.0687 g, 0.161 mmol) (Step 7, Example 252) in 1:1 EtOH-dioxane (8 mL) was added palladium, 10% wt. on activated carbon (0.007 g, 6.58 μmol) and hydrogenated (double-walled balloon pressure) at room temperature for 24 h. The reaction mixture was filtered via a pad of Celite, and the filtrate was concentrated in vacuo and purified via flash column chromatography (20% to 80% EtOAc (10% MeOH)/Hexanes) to give 4-(3-(4-(1H-benzo[d]imidazole-2-carbonyl)phenoxy)pyrazin-2-yl)-1-methylpiperidin-2-one (0.0262 g, 38.0% yield) as a light yellow amorphous solid. MS (ESI, pos. ion) m/z: 428.9 (M+1). IC50 (uM) +++++.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247418B2
Source datasetuspto-grants-2012_08
ORD IDord-8503ebfc40bb4e62bec432339ab9c07b
Source noteuspto-grants-2012_08