Réaction #2161257

ord-8ef16fb1b63747939cc2eae8138a3910

Équation de réaction

Cc1ccc(Cl)cn1
2-methyl-5-chloropyridine
CC(C)(C)OC(=O)N1CCNCC1
N-(tert-butyloxycarbonyl)piperazine
CC(C)(C)[O-].[Na+]
sodium tert-butoxide
c1ccc(P(c2ccccc2)c2ccc3ccccc3c2-c2c(P(c3ccccc3)c3ccccc3)ccc3ccccc23)cc1
BINAP
Cc1ccc(N2CCN(C(=O)OC(C)(C)C)CC2)nc1
1-(tert-Butyloxycarbonyl)-4-(5-methylpyridin-2-yl)piperazine

Conditions de réaction

Température
70°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureAfter cooling
  2. 2
    Lavagethe mixture is washed three times with a saturated sodium chloride solution
  3. 3
    Séchagedried over sodium sulfate
  4. 4
    Autrethe solvent is removed in vacuo
  5. 5
    AutreThe residue is purified by flash chromatography (cyclohexane/ethyl acetate 9:1)

Mode opératoire

Under an argon atmosphere, 2.50 g (19.6 mmol) of 2-methyl-5-chloropyridine and 4.38 g (23.5 mmol) of N-(tert-butyloxycarbonyl)piperazine are dissolved in 50 ml of absolute toluene. 2.26 g (23.5 mmol) of sodium tert-butoxide, 0.37 g (0.59 mmol) of BINAP and 0.36 g (0.39 mmol) of tris(dibenzylideneacetone)dipalladium are then added, and the mixture is heated at 70° C. for 12 h. After cooling, diethyl ether is added to the reaction mixture, the mixture is washed three times with a saturated sodium chloride solution and dried over sodium sulfate and the solvent is removed in vacuo. The residue is purified by flash chromatography (cyclohexane/ethyl acetate 9:1).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07919489B2uspto-grants-2011_04