4-Bromobenzaldehyde → 1,1-Dimethylethyl (2R,6S)-4-[(4-bromophenyl)methyl]-2,6-dimethyl-1-piperazinecarboxylate

HRID 43353

Reaktionsgleichung

Reaktionsgleichung von HRID 43353
[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][CH:3]=1.[CH3:10][C@@H:11]1[CH2:16][NH:15][CH2:14][C@H:13]([CH3:17])[N:12]1[C:18]([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C([O-])(O)=O.[Na+]>ClCCCl>[Br:1][C:2]1[CH:9]=[CH:8][C:5]([CH2:6][N:15]2[CH2:16][C@H:11]([CH3:10])[N:12]([C:18]([O:20][C:21]([CH3:22])([CH3:24])[CH3:23])=[O:19])[C@H:13]([CH3:17])[CH2:14]2)=[CH:4][CH:3]=1

Komponenten

6

Versuchsvorschrift

A mixture of 4-bromobenzaldehyde (1.85 g, 10 mmol), 1,1-dimethylethyl (2R,6S)-2,6-dimethyl-1-piperazinecarboxylate (2.15 g, 10 mmol) and sodium triacetoxyborohydride (3.18 g) in 1,2-DCE (35 ml) was stirred at room temperature for 3 days. Saturated aq. NaHCO3 solution was added and the mixture stirred for 30 mins. The product was extracted into EtOAc and the extracts dried (Na2SO4) and concentrated. The residue was dissolved in DCM and treated with PS-hydrazine resin with stirring for 2 h. The resin was removed by filtration and the solvent removed in vacuo. Chromatography (0-40% EtOAc/hexane) gave the title compound (3.52 g). MS (ES): MH+ 383/385.

Aufarbeitung

  1. stirringthe mixture stirred for 30 mins
  2. extractionThe product was extracted into EtOAc
  3. dry with materialthe extracts dried (Na2SO4)
  4. concentrationconcentrated
  5. dissolutionThe residue was dissolved in DCM
  6. additiontreated with PS-hydrazine resin
  7. stirringwith stirring for 2 h
  8. customThe resin was removed by filtration
  9. customthe solvent removed in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-758b8aff5c324789a35f03191e911f1b
Quelldatensatz
uspto-grants-2013_09
Patentnummer
US08536182B2

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