تفاعل #59656

ord-91dcda0975404d5b8b9d406eb83b22ee

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيز16 h at room temperature, the reaction mixture was concentrated
  2. 2
    workup.ADDITIONtreated with EtOAc and 6 N HCl (5 mL)
  3. 3
    تجفيفThe organic layer was dried over MgSO4
  4. 4
    تركيزconcentrated
  5. 5
    أخرىThe residue was purified by a silica gel column

الإجراء التجريبي

To a solution of 4-(2-Phenyl-cyclopropylcarbamoyl)-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester (422 mg, 1 mmol) in THF (2 mL) was added 1 N NaOH (1.5 mL) at 0° C. with stirring. After 30 min at 0° C. and 16 h at room temperature, the reaction mixture was concentrated and treated with EtOAc and 6 N HCl (5 mL). The organic layer was dried over MgSO4 and concentrated. The residue was purified by a silica gel column using CH2Cl2/MeOH (95:5) as eluant to yield the desired compound as a colorless oil (343 mg, 84%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07425633B2uspto-grants-2008_09