HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2090097Generated: October 31, 2026
HCID 25152788, compound → HCID 178439223, compound
https://huagongshe.com/reaction/2090097
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 25152788 | HCID 25152788 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178439223 | HCID 178439223 | 46.5% |
| Product | HCID 178439224 | HCID 178439224 | 39.5% |
Reaction Steps
To a solution of 4-(5-cyano-7-isopropyl-1,3-benzoxazol-2-yl)-N-{[4-(4-fluorophenyl)cyclohex-3-en-1-yl]methyl}benzamide (30 mg, 0.061 mmol, EXAMPLE 41) in methanol (1 ml) and tetrahydrofuran (1 ml) was added 10% palladium on carbon (10 mg, 0.094 mmol). The mixture was flushed with nitrogen, then flushed with hydrogen and stirred for 6 h under a hydrogen balloon, at which point LC/MS analysis showed no starting material. The mixture was added directly to a 1000-micron plate and then eluted with 1:1 ethyl acetate-hexanes to provide the desired products trans-4-(5-cyano-7-isopropyl-1,3-benzoxazol-2-yl)-N-{[4-(4-fluorophenyl)cyclohexyl]methyl}benzamide (11.9 mg, 0.024 mmol, 39.5% yield) and cis-4-(5-cyano-7-isopropyl-1,3-benzoxazol-2-yl)-N-{[4-(4-fluorophenyl)cyclohexyl]methyl}benzamide (14.0 mg, 0.028 mmol, 46.5% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08436028B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-3d3dc9c90b104accb5f7a21e8d96d2bb |
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| Source note | uspto-grants-2013_05 |
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