Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 3-Chloroaniline | HCID 7932 | — |
| Reactant | HCID 22137858 | HCID 22137858 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22137861 | HCID 22137861 | 92% |
Reaction Steps
To a CH2Cl2 solution of 2-Bromo-N-[3-(2-bromo-acetylamino)-5-trifluoromethyl-phenyl]-acetamide (150 mg, 0.30 mmol) at room temperature was added 3-chloroaniline (100 μL), the mixture was stirred at room temperature for 1 hour. The mixture was diluted with ethyl acetate, washed with NaHCO3 solution followed byl N HCl (2×) and brine. The organic layer was dried over MgSO4, filtered and stripped and the crude product was purified by flash chromatography on silica gel eluted with hexane/ethyl acetate (2:1) to give 132 mg of the title compound in 92% yield. 1H NMR (400 MHz, CDCl3): δ 3.87(s, 4H), 6.49(dd, J=2, 8.4 Hz, 2H), 6.63(s, 2H), 6.79(d, J=2, 8.4 Hz, 2H), 7.10(t, J=8.0 Hz, 2H), 7.46(s, 2H), 8.20(s, 1H), 8.77(s, 2H). MS SEI m/z relative intensity:M+H, 511.2(100).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07053234B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-63ca0ab73126474aadc7397dc001262a |
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| Source note | uspto-grants-2006_05 |
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