HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 59351234, compound → HCID 59351206, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 59351234 | HCID 59351234 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Dioxan ethanol | HCID 22560076 | — |
| Product | HCID 59351206 | HCID 59351206 | 38.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08247418B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-8503ebfc40bb4e62bec432339ab9c07b |
| Source note | uspto-grants-2012_08 |