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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985105Generated: October 29, 2026

Hydrochloric Acid → HCID 68536142, compound

https://huagongshe.com/reaction/1985105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantStannane, tributyl(1-ethoxyethenyl)-HCID 619414—
ReactantHCID 58909328HCID 58909328—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductHCID 68536142HCID 68536142—

Reaction Conditions

Temperature100 °C

Reaction Steps

To N-[(1S,2R)-3-{[(4-bromo-1,1′-biphenyl-2-yl)methyl]amino}-1-(3,5-difluorobenzyl)-2-hydroxypropyl]acetamide (120 mg, 0.24 mmol) in toluene (1 mL) was added tributyl(1-ethoxyvinyl)tin (100 μL, 0.28 mmol) and bis-triphenylphoshine palladium(II) dichloride (10 mg, 0.012 mmol), and the reaction was heated at 100° C. 3 h under N2. The solution was cooled to room temperature, 1N hydrochloric acid (1 mL) was added, and the mixture was stirred 20 min. The mixture was partitioned, and the organics were washed with saturated potassium fluoride (aq). The reaction mixture was dried (sodium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica gel, 8% methanol/methylene chloride) provided an oil. The residue was dissolved in ether, precipitated with excess 1N HCl in ether, and concentrated to provide the title compound (11 mg). ESI MS m/z 467.28 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544717B2
Source datasetuspto-grants-2009_06
ORD IDord-1c05855ff7ba486e933e887411fe645c
Source noteuspto-grants-2009_06