反応 #1790

ord-75cd419ae27e4e64877635a7083429d0

反応方程式

CC(C)(C)OC(=O)N[C@H]1CC[C@H](O)CC1
N-Boc-trans-1-amino-4-cyclohexanol
CCOC(=O)N=NC(=O)OCC
diethyl azodicarboxylate
COC(=O)c1ccc(O)cc1OC
methyl 4-hydroxy-2-methoxybenzoate
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
COC(=O)c1ccc(OC(=O)[C@H]2CC[C@@H](NC(=O)OC(C)(C)C)CC2)cc1OC
methyl 4-[N-Boc-cis-1-amino-4-cyclohexanoyloxy]-2-methoxybenzoate

溶媒

反応条件

温度
0°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過The reaction was filtered
  2. 2
    その他the solvent was removed under reduced pressure
  3. 3
    その他The residue was chromatographed on a silica gel column
  4. 4
    洗浄EtOAc and eluted with same
  5. 5
    その他the solvent removed under reduced pressure

実験手順

To a stirred solution of methyl 4-hydroxy-2-methoxybenzoate (1.09 g, 6.0 mmol) in dry THF (7 mL) was added triphenylphosphine (1.57 g, 6.0 mmol) and the solution was cooled to 0° C. A 4.0 mL volume of N-Boc-trans-1-amino-4-cyclohexanol (1 g, 4.0 mmol) and diethyl azodicarboxylate (945 μL, 6.0 mmol) in THF was added dropwise via addition funnel over 0.5 h. The reaction was filtered and the solvent was removed under reduced pressure. The residue was chromatographed on a silica gel column packed in 70:30 hexanes:EtOAc and eluted with same. The appropriate fractions were combined and the solvent removed under reduced pressure to afford methyl 4-[N-Boc-cis-1-amino-4-cyclohexanoyloxy]-2-methoxybenzoate.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05726172uspto-grants-1998_03