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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1724186Generated: October 26, 2026

Diisopropylethylamine → Methyl {1-[(4-chlorophenyl)(phenyl)methyl]azetidin-3-ylidene}(3,5-difluorophenyl)acetate

https://huagongshe.com/reaction/1724186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-[Bromo(phenyl)methyl]-4-chlorobenzeneHCID 11380508—
ReactantMethyl azetidin-3-yl(3,5-difluorophenyl)acetateHCID 67065947—
SolventAcetonitrileHCID 6342—
ProductMethyl {1-[(4-chlorophenyl)(phenyl)methyl]azetidin-3-ylidene}(3,5-difluorophenyl)acetateHCID 67065891—

Reaction Steps

A solution of 0.280 g (1 mmol) of 1-[bromo(phenyl)methyl]-4-chlorobenzene, 0.120 g (0.5 mmol) of methyl azetidin-3-yl(3,5-difluorophenyl)acetate (Example 22, Step 1) and 0.12 mL (0.7 mmol) of diisopropylethylamine in 10 mL of acetonitrile was heated at 40° C. for 18 h. The solution was concentrated and the residue was dissolved in 20 mL of ethyl acetate. This solution was washed with 10 mL water and the aqueous layer was washed with a second aliquot of 20 mL ethyl acetate. The organic extracts were washed with brine, combined, and concentrated. The residue was dissolved in acetonitrile and purified by reverse phase chromatography (Waters Xterra C18, 19 mm×50 mm) using a gradient of acetonitrile-water-triethylamine (30:70:1 to 60:40:1) to afford the title compound; 1NMR(CDCl3) δ 3.74 (s, 3H), 3.88 (m, 2H), 4.24 (m, 2H), 4.55 (s, 1H), 6.70-6.86 (m, 3H), 7.21-7.43 (m, 9H); Mass Spectrum: m/e=440 (M+1 35Cl) and 442 (M+1 37Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485732B2
Source datasetuspto-grants-2009_02
ORD IDord-1ef77606aa744fc48bc9a59f6632a5d4
Source noteuspto-grants-2009_02