HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810977Generated: November 1, 2026
HCID 59548815, compound → HCID 59548769, compound
https://huagongshe.com/reaction/1810977
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 59548815 | HCID 59548815 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59548769 | HCID 59548769 | 10.7% |
Reaction Steps
To a solution of 3-chloro-N-(5-chloro-2-{1-[2-(3,5-dimethyl-pyrazol-1-yl)-acetyl]-1,2,3,6-tetrahydro-pyridin-4-yl}-phenyl)-benzamide (0.100 g, 0.207 mmol) in ethanol (5 mL) is added Pd on 5% activated carbon (10 mg) in a round bottom flask and the mixture is purged three times and back filled with H2 using a H2 filled balloon. The reaction is allowed to stir at room temperature for 20 h. The reaction is filtered through a pad of diatomaceous earth and washed with MeOH. The filtrate is concentrated and purified via preparative HPLC. Removal of the solvent gives 0.010 g of N-(5-chloro-2-{1-[2-(3,5-dimethyl-pyrazol-1-yl)-acetyl]-piperidin-4-yl}-phenyl)-benzamide in 10% yield. MS MH+=450.2 and 0.030 g of N-(2-{1-[2-(3,5-Dimethyl-pyrazol-1-yl)-acetyl]-piperidin-4-yl}-phenyl)-benzamide in 35% yield. MS MH+=417.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362249B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-67f7ccf11f124c8e91dca00492df38d8 |
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| Source note | uspto-grants-2013_01 |
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