Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Reactant | 1-(4-Pyridyl)piperazine | HCID 70517 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18357115 | HCID 18357115 | 29.8% |
Reaction Steps
A solution of N-(4-pyridyl)piperazine (0.33 g) in dry dimethylformamide (15 ml) was treated with sodium hydride (0.14 g) (45-55% dispersion in oil). The reaction mixture was then stirred for 45 minutes at ambient temperature under argon. 4-Bromobenzyl bromide (0.58 g) was added and the mixture heated slowly to 60° C. and then maintained at this temperature for 2 hours. The resulting mixture was then poured into water, basified with aq.NaHCO3 solution and then extracted with diethyl ether. The organic extracts were then washed with aq.NaHCO3, water, brine, dried (Na2SO4) and evaporated. The residue was recrystallised from acetonitrile to give 1-(4-pyridyl)-4-(4-bromobenzyl)piperazine (0.2 g) as a solid, m.p. 140-141° C.; microanalysis, found: C,55.3; H,5.2; N,12.0%; C16H18N3Br requires: C,55.4; H,5.7; N,12.1%; NMR: (CDCl3) 2.54(t,4H); 3.2(t,4H); 3.51(s,2H); 6.66(d,2H); 7.23(d,2H); 7.46(d,2H); 8.29(d,2H); MS: m/z 332 (MH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06313127B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-ce13ed36ea2f4faeae2a8a7eba8699ac |
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| Source note | uspto-grants-2001_11 |
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