Reaktion #317767

ord-7919c91fd68a426cb45669c1a7f2747c

Reaktionsgleichung

CC(=O)c1ccc(NS(C)(=O)=O)c(C)c1
N-(4-acetyl-2-methylphenyl) methanesulfonamide
CC(C)(C)[S@](N)=O
(R)-(+)-2-methyl-2-propanesulfinamide
[BH4-].[Na+]
sodium borohydride
Cc1cc([C@@H](C)N[S@](=O)C(C)(C)C)ccc1NS(C)(=O)=O
title compound
Ausbeute 45.5%
Cc1cc([C@@H](C)N[S@](=O)C(C)(C)C)ccc1NS(C)(=O)=O
N-[4-((1R)-1-{[(R)-TERT-BUTYLSULFINYL]AMINO}ETHYL)-2-METHYLPHENYL]METHANESULFONAMIDE
Ausbeute 45.5%

Reaktionsbedingungen

Temperatur
70°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeIt was quenched with water
  2. 2
    Filtrationthe resulting white precipitate was filtered off
  3. 3
    SonstigeThe filtrate was partitioned between ethyl acetate and water
  4. 4
    TrocknenThe organic layer was dried over sodium sulfate
  5. 5
    Einengenconcentrated in vacuo
  6. 6
    SonstigeThe crude material was purified by silica gel column chromatography
  7. 7
    Wascheneluting with hexane/ethyl acetate (4:1)
  8. 8
    SonstigeThe yellow oil obtained
  9. 9
    Sonstigequenched with methanol
  10. 10
    workup.STIRRINGIt was stirred at room temperature for 1 hour
  11. 11
    Einengenconcentrated in vacuo

Vorschrift

To a solution of titanium(IV) ethoxide (1.32 g, 5.8 mol) and N-(4-acetyl-2-methylphenyl) methanesulfonamide (800 mg, 3.5 mmol) in tetrahydrofuran (20 mL) was added (R)-(+)-2-methyl-2-propanesulfinamide (423 mg, 350 mmol) under a nitrogen atmosphere and the mixture was heated at 70° C. for 16 hours. It was quenched with water and the resulting white precipitate was filtered off. The filtrate was partitioned between ethyl acetate and water. The organic layer was dried over sodium sulfate and concentrated in vacuo. The crude material was purified by silica gel column chromatography, eluting with hexane/ethyl acetate (4:1). The yellow oil obtained was dissolved in tetrahydrofuran (10 mL) and the solution was added to sodium borohydride (242 mg, 6.4 mmol) in tetrahydrofuran (10 mL) at −70° C. The mixture was stirred at −70° C. for 5 hours and then quenched with methanol. It was stirred at room temperature for 1 hour and concentrated in vacuo to furnish 530 mg (45%) of the title compound. MS (ESI) m/z 333 (M+H)+, 331 (M−H)−.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07566739B2uspto-grants-2009_07