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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749273Generated: October 30, 2026

Hydrochloric Acid → 4-(4-Fluorobenzyl)-3-(4-isobutoxybenzyl)-8-ethyl-1-oxa-3 8-diaza-spiro[4.5]decan-2-one, hydrochloride

https://huagongshe.com/reaction/749273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl BromideHCID 6332—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(4-Fluorobenzyl)-3-(4-isobutoxybenzyl)-2-oxo-1-oxa-3,8-diaza-spiro[4.5]decane-8-carboxylic acid tert-butyl esterHCID 57426041—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product4-(4-Fluorobenzyl)-3-(4-isobutoxybenzyl)-8-ethyl-1-oxa-3 8-diaza-spiro[4.5]decan-2-one, hydrochlorideHCID 131726973—

Reaction Steps

69NLS77 (190 mg, 0.45 mmol) was N-BOC deprotected as described in the preparation of 69NLS79-II and dissolved in DMF (3 mL). Potassium carbonate (250 mg, 1.80 mmol) was added, followed by ethylbromide (50 μL, 0.45 mmol)) and the mixture stirred overnight at rt. Workup was carried out as for 69NLS79-II. The residue was purified by silica gel column chromatography, eluting with a stepwise gradient of 0-6% methanol in dichloromethane, followed by repurification of the compound by acidic ion-exchange SPE cartridge, to give 38-PH20 (77 mg, 38%) as a colourless oil. The compound was converted to its hydrochloride form by treatment with 2M HCl in diethylether as described above, giving the salt as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402590B2
Source datasetuspto-grants-2008_07
ORD IDord-aa5ca4400bdd4e85a11db0f8ffafb822
Source noteuspto-grants-2008_07