反応 #1543047

ord-fdd83938c574463ba48ac845b07c1c2b

反応方程式

CC(C)(C)OC(=O)N[C@H](Cc1cccnc1)C(=O)O
Boc-D-Pal
CC(C)I
2-iodopropane
CC(C)I
2-iodopropane
CC(C)N1C=C(C[C@@H](NC(=O)OC(C)(C)C)C(=O)O)C=CC1
yellow oil
収率 78.3%
CC(C)N1C=C(C[C@@H](NC(=O)OC(C)(C)C)C(=O)O)C=CC1
Boc-D-Pal(iPr)
収率 78.3%

反応条件

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

後処理

  1. 1
    workup.ADDITIONAfter addition
  2. 2
    温度to warm to room temperature
  3. 3
    ろ過The mixture was filtered
  4. 4
    洗浄the precipitate was washed with ethanol (2×15 ml)
  5. 5
    その他The filtrate was evaporated

実験手順

Boc-D-Pal (4.0 g, 17.7 mmol) and Ag2O (8.0 g, 34.4 mmol) in 22 ml water was stirred at room temperature for 4 hours. The reaction vessel was cooled to 0° C., and 2-iodopropane (20.4 g, 120 mmol) in 40 ml 2-propanol was added. After addition was complete, the mixture was allowed to warm to room temperature and stirred for 4 days. Additional Ag2O (2 g) and 2-iodopropane (2 g) were added after 24 hours and again after 48 hours. The mixture was filtered, and the precipitate was washed with ethanol (2×15 ml). The filtrate was evaporated to yield 4.3 g of a yellow oil. Crystallization from ethanol/ethyl acetate gave light yellow crystals (3.0 g); Yield: 63%; m.p. 182°-185° C.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05843901uspto-grants-1998_12