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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170853Generated: October 31, 2026

Diisopropylethylamine → Benzo[d]isoxazol-3-yl(4-(4-chlorophenoxy)piperidin-1-yl)methanone

https://huagongshe.com/reaction/2170853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(4-Chlorophenoxy)piperidineHCID 5199889—
ReactantBenzo[d]isoxazole-3-carbonyl ChlorideHCID 10419807—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductBenzo[d]isoxazol-3-yl(4-(4-chlorophenoxy)piperidin-1-yl)methanoneHCID 6716879338.1%

Reaction Steps

To a solution of 4-(4-chlorophenoxy)piperidine (26 mg, 0.12 mmol), and N,N-diisopropylethylamine (0.086 mL, 0.49 mmol) in dichloromethane (0.5 mL) was added dropwise a solution of benzo[d]isoxazole-3-carbonyl chloride (22 mg, 0.12 mmol) in dichloromethane (0.5 mL) at room temperature. The reaction mixture was stirred at room temperature for 1 hour. The mixture was diluted with ethyl acetate (3 mL) and washed with water (1.5 mL). The organic layer was dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica-gel column chromatography (NH-gel, eluting with ethyl acetate) and then preparative LC-MS to give 16.3 mg (37% yield) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051296B2
Source datasetuspto-grants-2015_06
ORD IDord-36bcb924382c4a8db4d73e601405ff10
Source noteuspto-grants-2015_06