تفاعل #1253199

ord-f9f6c706e0294098a552464ab15a8d38

معادلة التفاعل

O=C1CN(c2ccc(N3C[C@H](CO)OC3=O)cc2F)CCN1CCF
(5R)-3-(3-Fluoro-4-[4-(2-fluoroethyl)-3-oxopiperazin-1-yl]phenyl)-5-hydroxymethyloxazolidin-2-one
CCN(CC)CC
Triethylamine
CS(=O)(=O)Cl
methanesulfonyl chloride
CS(=O)(=O)OC[C@H]1CN(c2ccc(N3CCN(CCF)C(=O)C3)c(F)c2)C(=O)O1
(5R)-3-(3-fluoro-4-[4-(2-fluoroethyl)-3-oxopiperazin-1-yl]phenyl)-5-(methanesulfonyloxymethyl)oxazolidin-2-one

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthe mixture cooled to 0°
  2. 2
    أخرىThe solvent is removed
  3. 3
    workup.DISSOLUTIONthe residue dissolved in dichloromethane
  4. 4
    غسيلwashed with water, saline
  5. 5
    تجفيفdried over magnesium sulfate
  6. 6
    تركيزconcentrated
  7. 7
    أخرىThe resulting residue is triturated with ether

الإجراء التجريبي

(5R)-3-(3-Fluoro-4-[4-(2-fluoroethyl)-3-oxopiperazin-1-yl]phenyl)-5-hydroxymethyloxazolidin-2-one (0.8 g) is dissolved in pyridine (15 ml) and the mixture cooled to 0°. Triethylamine (0.38 ml) and methanesulfonyl chloride (0.19 ml) are added to the mixture, and stirring continued at 20-25° for 2 hours. The solvent is removed and the residue dissolved in dichloromethane, washed with water, saline, dried over magnesium sulfate and concentrated. The resulting residue is triturated with ether to give (5R)-3-(3-fluoro-4-[4-(2-fluoroethyl)-3-oxopiperazin-1-yl]phenyl)-5-(methanesulfonyloxymethyl)oxazolidin-2-one (0.76 g) which is used without further purification.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06613349B2uspto-grants-2003_09