HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555830Generated: October 31, 2026
HCID 59351418, compound → HCID 59351345, compound
https://huagongshe.com/reaction/555830
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 59351418 | HCID 59351418 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59351345 | HCID 59351345 | — |
Reaction Steps
1H-Benzimidazol-2-yl(4-((3-(5,6-dihydro-2H-pyran-3-yl)-2-pyrazinyl)oxy)phenyl)methanone (0.20 g, 0.50 mmol) was suspended in 15 mL of EtOAc in a pressure tube. Palladium on carbon, 10% (0.20 g) was added. The mixture was hydrogenated at 50 psi. After 24 hours, the mixture was filtered through celite and eluted with 50 mL of 9:1 chloroform:isopropanol. The product was taken up in 10 mL of dichloromethane. Manganese dioxide (0.58 g, 6.7 mmol) was added. After 1 h, the mixture was filtered through celite and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (0 to 2% MeOH/dichloromethane) affording 1H-benzimidazol-2-yl(4-((3-(tetrahydro-2H-pyran-3-yl)-2-pyrazinyl)oxy)phenyl)methanone. MS (ESI, pos. ion) m/z: 401 (M+1). IC50 (uM) +++++.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08053438B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-de7aafd65cb6409b9b9e920413558ee5 |
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| Source note | uspto-grants-2011_11 |
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