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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691741Generated: October 26, 2026

Water → HCID 66906096, compound

https://huagongshe.com/reaction/1691741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 2-chloro-1,3-benzoxazole-5-carboxylateHCID 10774871—
Reactanttert-butyl {[3-(3-fluorophenyl)piperidin-4-yl]methyl}[(1R)-1-(1-naphthyl)ethyl]carbamateHCID 59178728—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 66906096HCID 6690609612.9%

Reaction Steps

To a solution of 185 mg of tert-butyl {[3-(3-fluorophenyl)piperidin-4-yl]methyl}[(1R)-1-(1-naphthyl)ethyl]carbamate in 2.00 mL of DMSO was added 18 mg of sodium hydride (55% dispersion) at room temperature, followed by stirring for 10 minutes. 89 mg of methyl 2-chloro-1,3-benzoxazole-5-carboxylate was added thereto, followed by stirring at 100° C. overnight. 55 mg of methyl 2-chloro-1,3-benzoxazole-5-carboxylate was further added thereto, followed by stirring at 100° C. overnight. The reaction mixture was cooled to room temperature, and water was then added thereto, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane-ethyl acetate and chloroform-methanol) to obtain 33 mg of methyl 2-[4-({(tert-butoxycarbonyl)[(1R)-1-(1-naphthyl)ethyl]amino}methyl)-3-(3-fluorophenyl)piperidin-1-yl]-1,3-benzoxazole-5-carboxylate as a colorless resinous compound. ESI+: 638

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153658B2
Source datasetuspto-grants-2012_04
ORD IDord-b5b780fd84e94752a85633da8eb79a51
Source noteuspto-grants-2012_04