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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350962Generated: October 31, 2026

Isopropanol → tert-butyl (1S)-1-(3,5-difluorobenzyl)-3-[(3-methoxybenzyl)amino]-2-oxopropylcarbamate

https://huagongshe.com/reaction/1350962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
Reactant1-Aminotetralin, (S)-HCID 7058074—
ReactantHCID 57484758HCID 57484758—
Producttert-butyl (1S)-1-(3,5-difluorobenzyl)-3-[(3-methoxybenzyl)amino]-2-oxopropylcarbamateHCID 86585851—

Reaction Steps

tert-butyl (1S)-3-bromo-1-(3,5-difluorobenzyl)-2-oxopropylcarbamate (III, EXAMPLE 1, 1 equivalent) is dissolved in isopropanol and treated with 3-methoxybenzylamine (VI, 5 equivalents). The reaction is heated at reflux for 2 hours and monitored by TLC for disappearance of the ketone (III). Upon completion, the reaction is concentrated to dryness under reduced pressure and partitioned between equal parts water and ethyl acetate. The organic phase is extracted, washed two additional times with water, then saline, then dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude material is purified by column chromatography on silica gel to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214715B2
Source datasetuspto-grants-2007_05
ORD IDord-21c0b6d1cd60402f96f20e8ceed06ab5
Source noteuspto-grants-2007_05