Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | 1-Benzoylpiperazine | HCID 762654 | — |
| Reactant | 4-Bromo-2-fluoro-1-nitrobenzene | HCID 2783362 | — |
| Reactant | Dimethylamine ethanol | HCID 22184060 | — |
| Reactant | HCID 67183248 | HCID 67183248 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 58425627 | HCID 58425627 | 21.2% |
Reaction Steps
A solution of 4-bromo-2-fluoro-1-nitrobenzene (1.0 g, 4.5 mmol) and 2.0 M dimethylamine ethanol solution (6.9 ml, 13.6 mmol) in 20 ml NMP was stirred at room temperature for 16 hours. The solution was added 200 ml water. The solids (1.03 g, 90%) were filtered dried under high vacuum. A solution of 5-bromo-N,N-dimethyl-2-nitrobenzenamine (0.2 g, 0.8 mmol), benzoyl piperazine (0.19 g, 1.0 mml), Tris(dibenzylideneacetone)dipalladium (9 mg), BINAP (38 mg) and cesium carbonate (0.24 g, 1.2 mmol) in 20 ml NMP was stirred at 100° C. under argon atmosphere for 16 hours. The reaction was cooled to room temperature before filtration. (4-(3-(dimethylamino)-4-nitrophenyl)piperazin-1-yl)(phenyl)methanone (0.06 g, 20%) was obtained after flash column chromatograph (50% ethyl acetate in hexanes). 1H NMR (500 MHz, CDCl3) δ (ppm) 2.93 (s, 6H), 3.40-3.57 (m, 8H), 6.26 (d, J=2.6 Hz, 1H), 6.35 (dd, J=2.6, 9.6 Hz, 1H), 7.48 (m, 5H), 7.98 (d, J=9.6 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08420640B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-5fac743b4a204abe8499bf548bf76517 |
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| Source note | uspto-grants-2013_04 |
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