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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927292Generated: November 3, 2026

Water → Methyl (2E)-3-{2-[(1R)-1-{[(2R)-3-[[1-(2,3-dihydro-1H-inden-2-yl)-2-methylpropan-2-yl]amino}-2-hydroxypropyl]oxy}ethyl]phenyl}prop-2-enoate

https://huagongshe.com/reaction/1927292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-(2,3-Dihydro-1H-inden-2-yl)-2-methylpropan-2-amineHCID 9834173—
ReactantLithium perchlorateHCID 23665649—
Reactantmethyl (2E)-3-(2-{(1R)-1-[(2R)-oxiran-2-yl methoxy]ethyl}phenyl)prop-2-enoateHCID 58662611—
SolventTolueneHCID 1140—
ProductMethyl (2E)-3-{2-[(1R)-1-{[(2R)-3-[[1-(2,3-dihydro-1H-inden-2-yl)-2-methylpropan-2-yl]amino}-2-hydroxypropyl]oxy}ethyl]phenyl}prop-2-enoateHCID 5857278437%

Reaction Steps

A mixture of methyl (2E)-3-(2-{(1R)-1-[(2R)-oxiran-2-yl methoxy]ethyl}phenyl)prop-2-enoate (342 mg, 1.30 mmol) described in WO 2004/106280, 1-(2,3-dihydro-1H-inden-2-yl)-2-methylpropan-2-amine (234 mg, 1.24 mmol) described in WO 01/53254, and lithium perchlorate (79 mg, 0.74 mmol) in toluene (12 mL) was stirred at room temperature for 16 hours. Water (10 mL) was added to the reaction solution, which was then extracted with ethyl acetate (10 mL×3). After that, the organic layers were combined, washed with saturated brine, and washed with anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate) to give the title compound as a colorless oily substance (206 mg, yield 37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183272B2
Source datasetuspto-grants-2012_05
ORD IDord-9aa67c9962274f48a0f8847a81e463d6
Source noteuspto-grants-2012_05