تفاعل #10519

ord-0671b17e79594082bfe04925787d737d

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحThe catalyst was filtered off through kieselguhr
  2. 2
    غسيلthe filter cake was washed with 20 ml of acetic acid
  3. 3
    تركيزThe combined organic phases were concentrated in vacuo
  4. 4
    أخرىThe crude product was employed without further purification in the next reaction

الإجراء التجريبي

1600 mg of (2S,5S)-5-(2-benzylamino-2-carboxyethyl)pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester were dissolved in 30 ml of acetic acid. 100 mg of 20% palladium hydroxide on activated carbon were added thereto, and the mixture was hydrogenated under an atmosphere of 1 bar of hydrogen for 1 h. Ar was then passed over the solution for 10 min. The catalyst was filtered off through kieselguhr and the filter cake was washed with 20 ml of acetic acid. The combined organic phases were concentrated in vacuo. The crude product was employed without further purification in the next reaction.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07094800B2uspto-grants-2006_08