HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850790Generated: October 30, 2026
HCID 86711207, compound → HCID 86711208, compound
https://huagongshe.com/reaction/1850790
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86711207 | HCID 86711207 | — |
| Reactant | HCID 178496050 | HCID 178496050 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86711208 | HCID 86711208 | — |
Reaction Steps
To a solution of 4-((1R,2S)-2-{2-{2-fluoro-4-(methylsulfonyl)phenoxy]ethyl}cyclopropyl)piperidine-1-carbonitrile (Step D, Example 111; 100 mg, 0.27 mmol) and N-hydroxy-2-methoxyacetimidamide (38 mg, 0.37 mmol) in tetrahydrofuran (5 mL) was added zinc chloride (0.8 mL, 0.5 M in tetrahydrofuran, 0.4 mmol). The mixture was refluxed for 2 h, cooled to RT, and concentrated to dryness under reduced pressure. The residue was dissolved in 2 mL of 4N HCl ethanol and water (1:1). The solution was refluxed for 30 min, cooled to RT, and concentrated to dryness under reduced pressure. The residue was dissolved in methanol (5 mL), neutralized by the addition of excess potassium carbonate, mixed silica gel (2 g), and concentrated to dryness under reduced pressure. The residue was loaded on a silica gel column (10 g of silica gel) and eluted with a gradient of dichloromethane/CMA, 19:1, 500 mL; 4:1, 500 mL to provide the title compound. MS (ESI) m/z 454 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957062B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-4ca24d07ce524cad8ca603b7e6b8a939 |
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| Source note | uspto-grants-2015_02 |
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