반응 #657274

ord-416c43870ebc4b539910d8c288581fe0

반응 방정식

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

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwere added to the residue
  2. 2
    여과The solution was filtered
  3. 3
    기타the filtrate was evaporated in vacuo to dryness
  4. 4
    기타The product was recrystallised from diisopropylether

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09023656B2uspto-grants-2015_05