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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219094Generated: October 31, 2026

Water → HCID 18510681, compound

https://huagongshe.com/reaction/2219094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHCID 9820758HCID 9820758—
ReactantHCID 178418332HCID 178418332—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18510681HCID 1851068150%

Reaction Conditions

Temperature0 °C

Reaction Steps

) CH3MgCl, 22% (w/w)/THF (0.003 mol) was added dropwise to a cooled (0° C.) solution of (±)-N-(4-benzoylphenyl)-4,5-dihydro-3-(3-pyridinyl)-5-isoxazolecarboxamide (0.003 mol) in THF (50 ml). The reaction mixture was stirred for 30 minutes at 0° C. More CH3MgCl, 22% w/w/THF (0.003 mol) was added and the mixture was stirred for 30 minutes at 0° C. Extra CH3MgCl, 22% (w/w)/THF (0.003 mol) was added and the reaction mixture was stirred for 30 minutes at 0° C. The mixture was allowed to warm to RT for 30 minutes, then cooled again to 0° C. Water was added. This mixture was extracted with CH2Cl2. The separated organic layer was dried (MgSO4), filtered and the solvent evaporated under reduced pressure. The crude oil was crystallized from EtOAc. The precipitate was filtered off, washed with EtOAc, and dried, yielding 0.5 g(50%) of (±)4,5-dihydro-N-[4-(1-hydroxy-1-phenylethyl)phenyl]-3-(3-pyridinyl)-5-isoxazolecarboxamide (compound 51).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07414048B2
Source datasetuspto-grants-2008_08
ORD IDord-9d874e7096ea41a18ed4ac8db985fe81
Source noteuspto-grants-2008_08