Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Tolylboronic acid | HCID 79799 | — |
| Reactant | HCID 59853713 | HCID 59853713 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 59853655 | HCID 59853655 | — |
Reaction Steps
In analogy to a procedure described by Leadbeater et al. [N.E. Leadbeater, M. Marco, Org. Lett. 4, 2973 (2002)] a stirred mixture of 1 eq. 1-{4-[4-(2-bromo-5-nitro-benzoyl)-piperazin-1-yl]-3-fluoro-phenyl}-ethanone (Example 4), 1.05 eq. 4-methylphenylboronic acid, 1 eq. tetrabutylammonium bromide. 2.5 eq. sodium carbonate and 0.01 eq Pd(OAc)2 in water (20 ml per mmol) were heated in a sealed tube to 150° C. by microwave irradiation for 1 minute. Then the reaction mixture is diluted with water, extracted with AcOEt, the pooled organic extracts dried over Na2SO4, filtered and evaporated. The crude product is purified by preparative HPLC on a YMC Combiprep ODS-AQ column with an acetonitrile/water+0.1% formic acid gradient to yield the title compound (table 2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07462617B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-392a3c1f259b4d0c87219c0a2eeca389 |
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| Source note | uspto-grants-2008_12 |
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