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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370259Generated: October 31, 2026

Water → HCID 18510695, compound

https://huagongshe.com/reaction/1370259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 53672405HCID 53672405—
ReactantHCID 86590905HCID 86590905—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 18510695HCID 1851069535%

Reaction Conditions

Temperature0 °C

Reaction Steps

) Intermediate (3) (0.007 mol) was added to a solution of methyl [(4-aminophenyl) phenyl]acetate (0.007 mol), N,N-bis(1-methylethyl)ethanamine (0.014 mol) and N,N-dimethyl-4-pyridinamine (catalytic quantity) in CH2Cl2 (100 ml), stirred at 0° C. The reaction mixture was stirred overnight at RT. Water was added. The organic layer was separated, dried (MgSO4), filtered and the solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography over silica gel (eluent: CH2Cl2/CH3OH 98/2). The pure fractions were collected and the solvent was evaporated under reduced pressure. The residue was crystallized from EtOAc. The precipitate was filtered off, washed with EtOAc, and dried, yielding 1.0 g (35%) of (±)-methyl 4-[[[4,5-dihydro-3-(3-pyridinyl)-5-isoxazolyl]carbonyl]amino]-α-phenylbenzeneacetate (compound 56).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583141B1
Source datasetuspto-grants-2003_06
ORD IDord-21193f42678c43e4aa608aa693a6ef14
Source noteuspto-grants-2003_06