تفاعل #93118
ord-c7f8efba479f491d855bc32b4e942921
معادلة التفاعل
المتفاعلات
الكواشف
لا شيء
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1workup.ADDITIONafter adding slowly
- 2درجة الحرارةcooling
- 3درجة الحرارةcooling
- 4أخرىPrecipitates
- 5ترشيحwere filtered off
- 6تركيزthe filtrate was concentrated
- 7أخرىthe residue thus formed
- 8غسيلBy eluting the product with ethyl acetatemethanol (4:1)
الإجراء التجريبي
In 100 ml of THF was dissolved 9.97 g of compound (29) and after adding slowly thereto 4.45 g of triethylamine and then 6.01 g of isobutyl chloroformate under ice-cooling, the reaction was performed under ice-cooling. To the reaction mixture was slowly added 11.37 g of 3-(2-oxo-1-pyrrolidinyl)-propylamine and then the reaction was performed for one hour under ice-cooling. Precipitates were filtered off, the filtrate was concentrated, and the residue thus formed was subjected to silica gel column chromatography. By eluting the product with ethyl acetatemethanol (4:1), 4.43 g of (S)-1-benzyloxycarbonyl-N-[3-(2-oxo-pyrrolidinyl)propyl]-2-pyrrolidine carboxamide (99) was obtained.