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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409986Generated: October 28, 2026

Triethylamine → 6-Chlorobenzo[d]isoxazol-3-yl 4-methylpiperidine-1-carboxylate

https://huagongshe.com/reaction/1409986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Methylpiperidine-1-carbonyl ChlorideHCID 15221516—
ReactantHCID 178518989HCID 178518989—
SolventPyridineHCID 1049—
Product6-Chlorobenzo[d]isoxazol-3-yl 4-methylpiperidine-1-carboxylateHCID 12001416—

Reaction Steps

200 mg (1.18 mmol) of 6-chlorobenzo[d]isoxazol-3-ol, 228.7 mg (1.41 mmol) of 4-methylpiperidine-1-carbonyl chloride and 164 μl (2.36 mmol) of triethylamine were dissolved in 10 ml of pyridine and stirred at room temperature for 24 h. The reaction mixture was concentrated, and the residue was dissolved in water and extracted with ethyl acetate. The organic phase was concentrated and purified by preparative HPLC (PR18, acetonitrile/water 0.1% TFA). Yield: 147 mg (42%), M+H+: 295.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921404B2
Source datasetuspto-grants-2014_12
ORD IDord-3010e090d5c64ce6b53f16ac35506f09
Source noteuspto-grants-2014_12