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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850790Generated: October 30, 2026

HCID 86711207, compound → HCID 86711208, compound

https://huagongshe.com/reaction/1850790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86711207HCID 86711207—
ReactantHCID 178496050HCID 178496050—
CatalystZincchlorideHCID 3007855—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86711208HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957062B2
Source datasetuspto-grants-2015_02
ORD IDord-4ca24d07ce524cad8ca603b7e6b8a939
Source noteuspto-grants-2015_02