反応 #10170

ord-0300c97a88a5417abebd157852f56576

反応方程式

CCN=C=NCCCN(C)C
1-ethyl-3-(3-dimethylaminopropyl)carbodiimide
N[C@@]12C[C@H]1COC2=O
(±)-Trans-1-amino-3-oxabicyclo[3.1.0]hexan-2-one
O=C(O)CC(F)(F)F
3,3,3-trifluoropropionic acid
Oc1cccc2[nH]nnc12
Hydroxybenzotriazole
O=C(CC(F)(F)F)N[C@@]12C[C@H]1COC2=O
3,3,3-trifluoro-N-[(±)-trans-2-oxo-3-oxabicyclo[3.1.0]hex-1-yl]-propanamide
収率 45.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    抽出the reaction mixture was extracted with ethyl acetate
  2. 2
    洗浄The combined organic extracts were washed with water and brine
  3. 3
    乾燥dried (sodium sulfate)
  4. 4
    濃縮concentrated
  5. 5
    その他to give the crude product
  6. 6
    その他This was purified by silica gel chromatography

実験手順

(±)-Trans-1-amino-3-oxabicyclo[3.1.0]hexan-2-one (128 mg, 1.13 mmol) was mixed with 3,3,3-trifluoropropionic acid in 2.3 mL of N,N-dimethylformamide. Hydroxybenzotriazole (17.4 mg, 0.11 mmol) was added followed by 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (282 mg, 1.47 mmol). The pH of the reaction mixture was adjusted to 8.5 with triethylamine and the mixture was allowed to stir at ambient temperature for 2 hours. Water was then added and the reaction mixture was extracted with ethyl acetate. The combined organic extracts were washed with water and brine, then dried (sodium sulfate) and concentrated to give the crude product. This was purified by silica gel chromatography to afford 120 mg (45%) of 3,3,3-trifluoro-N-[(±)-trans-2-oxo-3-oxabicyclo[3.1.0]hex-1-yl]-propanamide.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07091380B2uspto-grants-2006_08