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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460564Generated: October 25, 2026

(S)-(+)-Glycidyl-4-nitrobenzoate → ethyl (S)-4-(2-hydroxy-3-(4-(naphthalen-2-yl)piperidino)propyloxy)-1-(2-methylpropyl)indole-2-carboxylate

https://huagongshe.com/reaction/460564

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-(+)-Glycidyl-4-nitrobenzoateHCID 10868995—
Reactant4-(Naphthalen-2-yl)piperidineHCID 22029264—
ReactantEthyl 4-hydroxy-1-(2-methylpropyl)indole-2-carboxylateHCID 22728995—
Productethyl (S)-4-(2-hydroxy-3-(4-(naphthalen-2-yl)piperidino)propyloxy)-1-(2-methylpropyl)indole-2-carboxylateHCID 8658564181.7%

Reaction Steps

By the reactions in the same manner as in Starting Material Synthesis Example 25 using ethyl 4-hydroxy-1-(2-methylpropyl)indole-2-carboxylate (5.0 g) obtained in Starting Material Synthesis Example 12, (S)-glycidyl nosylate (4.5 g) and 4-(naphthalen-2-yl)piperidine (5.3 g), ethyl (S)-4-(2-hydroxy-3-(4-(naphthalen-2-yl)piperidino)propyloxy)-1-(2-methylpropyl)indole-2-carboxylate (7.5 g) was obtained. This was dissolved in ethanol (40 ml) and water (30 ml) and potassium hydroxide (4.0 g) were added. The mixture was refluxed for 2.5 hr. From the obtained reaction mixture, ethanol was evaporated under reduced pressure and 1N aqueous hydrochloric acid solution (30 ml) was added under ice-cooling. The mixture was extracted with chloroform. The obtained organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and isopropyl ether was added to the obtained oil. The obtained crystals were collected by filtration to give the title compound (6.7 g) as pale-yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196199B2
Source datasetuspto-grants-2007_03
ORD IDord-fce260f4538047b79c9d27d1079688cb
Source noteuspto-grants-2007_03