تفاعل #77838

ord-945bbde546ad490c90d9d0f5dce0de13

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلThe EtOAc layer was washed with 1 N HCl, NaHCO3 solution, and brine
  2. 2
    تجفيفThe EtOAc was dried (MgSO4)
  3. 3
    ترشيحfiltered
  4. 4
    تركيزconcentrated to a solid (2.6 g)
  5. 5
    workup.DISSOLUTIONThis solid was dissolved in MeOH (14 mL)
  6. 6
    workup.ADDITIONto the addition of 10% Pd/C
  7. 7
    workup.ADDITIONA hydrogen balloon was added
  8. 8
    workup.STIRRINGthe solution was stirred for 1 h
  9. 9
    ترشيحThe palladium was filtered
  10. 10
    تركيزthe solution was concentrated

الإجراء التجريبي

2-(Pyrrolidinylcarbonyl)amino-5-trifluoromethylbenzoic acid (made analogously to Example 116 with pyrrolidine in place of iso-butylamine (2.9 g) was dissolved in DMF (40 mL). After cooling to 0° C., 4-methylmorpholine (3.2 mL) and glycine benzyl ester hydrogen chloride (5.6 g) were added. After 5 min, BOP Reagent (5.6 g) was added and the mixture was stirred at rt for 18 h. EtOAc was added along with 1 N HCl solution. The EtOAc layer was washed with 1 N HCl, NaHCO3 solution, and brine. The EtOAc was dried (MgSO4), filtered, and concentrated to a solid (2.6 g). This solid was dissolved in MeOH (14 mL) prior to the addition of 10% Pd/C. A hydrogen balloon was added and the solution was stirred for 1 h. The palladium was filtered and the solution was concentrated to give the title glycine derivative (2.0 g) as a white solid. MS found: (M+H)+=360.2.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06706712B2uspto-grants-2004_03