تفاعل #1272

ord-2d46e70de5c24d3e972efa60da2d0c9b

معادلة التفاعل

CN(C)NCCCC[C@H](NC(=O)OCc1ccccc1)C(=O)OC(C)(C)C
dimethylamine
CN(C)NCCCC[C@H](NC(=O)OCc1ccccc1)C(=O)OC(C)(C)C
Nε-dimethylamino-Nα-CBZ-O-t-butyl L-lysine
OO
hydrogen peroxide
OO
hydrogen peroxide
CN(C)NCCCC[C@@H](C(=O)OC(C)(C)C)[NH+]([O-])C(=O)OCc1ccccc1
product
CN(C)NCCCC[C@@H](C(=O)OC(C)(C)C)[NH+]([O-])C(=O)OCc1ccccc1
Nε-dimethylamino-Nα-CBZ-O-t-butyl L-lysine N-oxide

المذيبات

ظروف التفاعل

درجة الحرارة
60°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added
  2. 2
    غسيلeluting with solvent A
  3. 3
    workup.ADDITIONA 1 mL aqueous slurry of approximately 5 mg of platinum black was added whereupon the reaction
  4. 4
    workup.STIRRINGwas stirred for 7 h
  5. 5
    workup.ADDITIONanother slurry of 5-10 mg platinum black added
  6. 6
    workup.STIRRINGThe mixture was stirred overnight
  7. 7
    أخرىto remove peroxides when necessary
  8. 8
    ترشيحthe mixture was filtered
  9. 9
    تركيزconcentrated
  10. 10
    workup.DISSOLUTIONThe residue was dissolved into 300 mL of EtOAc
  11. 11
    تجفيفdried over Na2SO4
  12. 12
    ترشيحfiltered
  13. 13
    تركيزconcentrated
  14. 14
    أخرىchromatographed on 400 g of silica gel
  15. 15
    غسيلeluting with Solvent A

الإجراء التجريبي

A solution of 25.3 g of dimethylamine 2, 7.9 mL of 30% hydrogen peroxide and 150 mL of methanol was stirred for 5 h after which an additional 7.9 g of 30% hydrogen peroxide was added. The reaction was allowed to stir for 48 h and monitored by silica gel TLC, eluting with solvent A. A 1 mL aqueous slurry of approximately 5 mg of platinum black was added whereupon the reaction was stirred for 7 h and another slurry of 5-10 mg platinum black added. The mixture was stirred overnight and monitored for peroxides using peroxide test paper with warming to 60° C. to remove peroxides when necessary. Once the reaction tested negative for peroxides, the mixture was filtered and concentrated. The residue was dissolved into 300 mL of EtOAc, dried over Na2SO4, filtered, concentrated and chromatographed on 400 g of silica gel, eluting with Solvent A to produce 13 g of product as a colorless oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05723619uspto-grants-1998_03