반응 #5826

ord-5e959f0c247e4beda9969377311282aa

반응 방정식

CC(C)(C)OC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)O
N-tert-butoxycarbonyltyrosine
O=C(OCc1ccccc1)N1CCCNCC1
N-benzyloxycarbonylhomopiperazine
O.On1nnc2ccccc21
1-hydroxybenzotriazole hydrate
C(=NC1CCCCC1)=NC1CCCCC1
DCC
CC(C)(C)OC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N1CCCN(C(=O)OCc2ccccc2)CC1
title compound
수율 97.7%
CC(C)(C)OC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N1CCCN(C(=O)OCc2ccccc2)CC1
1-Benzyloxycarbonyl-4-(N-Tert-Butoxycarbonyltyrosyl)Homopiperazine
수율 97.7%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGthe reaction mixture was stirred for 16 hours
  2. 2
    기타The reaction mixture was evaporated
  3. 3
    기타to remove the solvent under a reduced pressure
  4. 4
    workup.ADDITIONto the residue was added benzene, and insoluble matter
  5. 5
    여과was filtered by suction
  6. 6
    세척washed with benzene
  7. 7
    기타evaporated off under a reduced pressure
  8. 8
    세척eluted with chloroform/methanol (100:1)

실험 절차

15.29 g of N-tert-butoxycarbonyltyrosine and 12.73 g of N-benzyloxycarbonylhomopiperazine were dissolved in 280 ml of tetrahydrofuran, to the solution were added 8.09 g of 1-hydroxybenzotriazole hydrate and 11.77 g of DCC at a room temperature with stirring, and the reaction mixture was stirred for 16 hours. The reaction mixture was evaporated to remove the solvent under a reduced pressure, to the residue was added benzene, and insoluble matter was filtered by suction and washed with benzene. The benzene layers were combined and evaporated off under a reduced pressure. The resulting residue was applied to a silica gel column and eluted with chloroform/methanol (100:1), to obtain 26.42 g of the title compound in colorless amorphous form.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05245034uspto-grants-1993_09