تفاعل #657274

ord-416c43870ebc4b539910d8c288581fe0

معادلة التفاعل

Cc1ccc(S(=O)(=O)O)cc1
p-toluenesulphonic acid
CC(NC(=O)CN1C(C)CCCC1C)C(=O)O
2-[2-(2,6-Dimethyl-piperidin-1-yl) acetylamino]-propanoic acid
CC(NC(=O)CN1C(C)CCCC1C)C(=O)O
2-[2-(2,6-Dimethyl-piperidin-1-yl)acetylamino]-propanoic acid
O=C1CCC(=O)N1O
N-Hydroxysuccinimide
C(=NC1CCCCC1)=NC1CCCCC1
N,N′-Dicyclohexylcarbodiimide
CC(NC(=O)CN1C(C)CCCC1C)C(=O)ON1C(=O)CCC1=O
2-[2-(2,6-Dimethyl-piperidin-1-yl)acetylamino]-propanoic acid-(2,5-dioxo-pyrrolidine-1-yl)-ester

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwere added to the residue
  2. 2
    ترشيحThe solution was filtered
  3. 3
    أخرىthe filtrate was evaporated in vacuo to dryness
  4. 4
    أخرىThe product was recrystallised from diisopropylether

الإجراء التجريبي

4.75 g (25 mMol) p-toluenesulphonic acid were heated under reflux for 1 h in 20 ml toluene using a water separator. After having evaporating the solvent, 6.30 g (25 mMol) 2-[2-(2,6-Dimethyl-piperidin-1-yl) acetylamino]-propanoic acid (27), 2.88 g (25 mMol) N-Hydroxysuccinimide and 5.15 g (25 mMol) N,N′-Dicyclohexylcarbodiimide were added to the residue dissolved in 100 ml dichloromethane. The reaction mixture was stirred for 16 h at room temperature. The solution was filtered and the filtrate was evaporated in vacuo to dryness. The product was recrystallised from diisopropylether.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09023656B2uspto-grants-2015_05