تفاعل #159165

ord-908c5677004f4da3911155097c454f59

المذيبات

ظروف التفاعل

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

المعالجة

  1. 1
    ترشيحwas filtered over elite
  2. 2
    تركيزThe filtrate was concentrated to a residue which
  3. 3
    workup.DISSOLUTIONwas dissolved in diethyl ether
  4. 4
    غسيلThe organic solution was washed with 10% HCl and brine
  5. 5
    تجفيفdried over MgSO4
  6. 6
    ترشيحfiltered
  7. 7
    تركيزconcentrated
  8. 8
    أخرىThe crude residue was purified by silica column chromatography (20% to 80% EtOAc/Hex)

الإجراء التجريبي

4-Hydroxymethyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester (861 mg, 3.32 mmol) was dissolved in DCM (6.6 mL) then 2,6-di-tert-butyl-4-methylpyridine (1.023 g, 4.98 mmol) and AgOTf (938 mg, 3.65 mmol) were added. The reaction mixture was cooled to 0° C. and iodomethane (0.25 mL, 3.98 mmol) was added. After 4 min, the reaction mixture was diluted with DCM and it was filtered over elite. The filtrate was concentrated to a residue which was dissolved in diethyl ether. The organic solution was washed with 10% HCl and brine, then dried over MgSO4, filtered and concentrated. The crude residue was purified by silica column chromatography (20% to 80% EtOAc/Hex) to afford the title compound (479 mg, 53%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08822430B2uspto-grants-2014_09