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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1724212Generated: November 3, 2026

Diisopropylethylamine → HCID 57559933, compound

https://huagongshe.com/reaction/1724212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-[Bromo(4-chlorophenyl)methyl]benzonitrileHCID 67055351—
Reactant1-Azetidin-3-yl-1-(3,5-difluorophenyl)-2,2-dimethylpropan-1-olHCID 67065942—
SolventAcetonitrileHCID 6342—
ProductHCID 57559933HCID 57559933—

Reaction Steps

The reaction mixture of 135 mg (0.44 mmol) of 3-[bromo(4-chlorophenyl)methyl]benzonitrile, 105 mg (0.367 mmol) of 1-azetidin-3-yl-1-(3,5-difluorophenyl)-2,2-dimethylpropan-1-ol (3) and 230 uL (1.32 mmol) of N,N-diisopropylethylamine in 6 mL of acetonitrile was refluxed for 3 h. Then it was concentrated and the residue was dissolved in 5 mL of hexane/ether. 1 mL of 1N HCl in ether was added to above solution to make salt. It was filtered and washed with hexane/ether. The residue was neutralized with base and was purified by silica gel chromatography with hexanes/ethyl acetate to afford one racemic diastereomer of the title compound; Mass Spectrum: m/e=481 (M+1 35Cl) and 483 (M+1 37Cl). Further elution of the column afforded the other racemic diastereomer of the title compound; Mass Spectrum: m/e=481 (M+1 35Cl) and 483 (M+1 37Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485732B2
Source datasetuspto-grants-2009_02
ORD IDord-b3df6b25d90a4c94bd5ae8eb4c816346
Source noteuspto-grants-2009_02