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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-[Bromo(phenyl)methyl]-4-chlorobenzene | HCID 11380508 | — |
| Reactant | Methyl azetidin-3-yl(3,5-difluorophenyl)acetate | HCID 67065947 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl {1-[(4-chlorophenyl)(phenyl)methyl]azetidin-3-ylidene}(3,5-difluorophenyl)acetate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07485732B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-1ef77606aa744fc48bc9a59f6632a5d4 |
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| Source note | uspto-grants-2009_02 |
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