تفاعل #1519113

ord-8380122c7f21428eb5264a0946a1d997

معادلة التفاعل

COC(=O)CBr
methyl bromoacetate
CCCCCC(=O)N1C(=O)OC[C@@H]1Cc1ccccc1
N-hexanoyl-4-(S)-benzyloxazolidin-2-one
C[Si](C)(C)[N-][Si](C)(C)C.[Na+]
NaHMDS
CCCC[C@H](CC(=O)OC)C(=O)N1C(=O)OC[C@@H]1Cc1ccccc1
methyl 3-(R)-(n-butyl)-3-[4-(S)-benzyloxazolidin-2-one-3-ylcarbonyl)propionate

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
-78°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGthe resulting mixture is stirred at −78° C. for 1 hour
  2. 2
    أخرىat rt
  3. 3
    أخرىovernight
  4. 4
    أخرىThe reaction is quenched with NH4Cl
  5. 5
    تركيزconcentrated
  6. 6
    غسيلwashed with 0.5 N HCl and brine
  7. 7
    أخرىdried
  8. 8
    أخرىpurified by silica gel chromatography (EtOAc/hexanes)

الإجراء التجريبي

To a solution of N-hexanoyl-4-(S)-benzyloxazolidin-2-one A-2 (7.3 mmol) in THF at −78° C. is added 1.0 M NaHMDS (8.8 mmol) and the reaction stirred at −78° C. for 1 hour. A solution of methyl bromoacetate (8.8 mmol) in THF is then added dropwise, and the resulting mixture is stirred at −78° C. for 1 hour and then at rt overnight. The reaction is quenched with NH4Cl, concentrated, then suspended in EtOAc and washed with 0.5 N HCl and brine, dried and purified by silica gel chromatography (EtOAc/hexanes) to afford the methyl 3-(R)-(n-butyl)-3-[4-(S)-benzyloxazolidin-2-one-3-ylcarbonyl)propionate (A-3).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07612059B2uspto-grants-2009_11