반응 #41907

ord-1cad58ca94e541a28a7f5dd0fffe7af6

반응 방정식

COC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)OC(C)(C)C
(S)-2-tert-Butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionic acid methyl ester
OB(O)c1ccncc1
4-pyridyl boronic acid
CCN(CC)CC
Triethylamine
COC(=O)[C@H](Cc1ccc(Oc2ccncc2)cc1)NC(=O)OC(C)(C)C
(S)-2-tert-Butoxycarbonylamino-3-[4-(pyridin-4-yloxy)-phenyl]-propionic acid methyl ester
수율 20.7%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척washed with 10% sodium carbonate (6×)
  2. 2
    기타The organic layer was dried
  3. 3
    농축concentrated under reduced pressure
  4. 4
    기타The residue was purified over silica gel (hexanes-EtOAc)

실험 절차

(S)-2-tert-Butoxycarbonylamino-3-(4-hydroxy-phenyl)-propionic acid methyl ester (8.46 mmol), 4-pyridyl boronic acid (29.6 mmol), Cu(OAc)2 (16.9 mmol), and molecular sieves were suspended in 25 mL of DCM. Triethylamine (59.2 mmol) was added and the mixture stirred at rt for 10 h. The mixture was diluted with ethyl acetate and washed with 10% sodium carbonate (6×). The organic layer was dried and concentrated under reduced pressure. The residue was purified over silica gel (hexanes-EtOAc) to provide (S)-2-tert-Butoxycarbonylamino-3-[4-(pyridin-4-yloxy)-phenyl]-propionic acid methyl ester (653 mg). LC-MS (m/z) 374.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07727983B2uspto-grants-2010_06