反応 #2186173

ord-897ac175caba43478a3e13f2ff0120fa

反応方程式

N[C@@H](CSCC(O)CO)C(=O)O
S-(2,3-dihydroxypropyl)cysteine
O=C(OCc1cccc2c1Cc1ccccc1-2)C1CC(=O)N(O)C1=O
fluorenylmethoxycarbonyl-N-hydroxysuccinimide
O=C(N[C@@H](CSCC(O)CO)C(=O)O)OCc1cccc2c1Cc1ccccc1-2
powder
収率 63.8%
O=C(N[C@@H](CSCC(O)CO)C(=O)O)OCc1cccc2c1Cc1ccccc1-2
N-Fluorenylmethoxycarbonyl-S-(2,3-dihydroxypropyl)cysteine
収率 63.8%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    抽出extracted with diethyl ether (25 ml×3)
  2. 2
    抽出was then extracted with ethyl acetate (70 ml×3)
  3. 3
    洗浄The extract was washed with water (50 ml×2) and saturated sodium chloride solution (50 ml×2)
  4. 4
    乾燥dried over sodium sulfate
  5. 5
    その他evaporated to dryness
  6. 6
    その他Recrystalisation from ether and ethyl acetate at −20° C.

実験手順

S-(2,3-dihydroxypropyl)cysteine (2.45 g, 12.6 mmole) was dissolved in 9% sodium carbonate (20 ml). A solution of fluorenylmethoxycarbonyl-N-hydroxysuccinimide (3.45 g, 10.5 mmole) in acetonitrile (20 ml) was added and the mixture stirred for 2 h, then diluted with water (240 ml), and extracted with diethyl ether (25 ml×3). The aqueous phase was acidified to pH 2 with concentrated hydrochloric acid and was then extracted with ethyl acetate (70 ml×3). The extract was washed with water (50 ml×2) and saturated sodium chloride solution (50 ml×2), dried over sodium sulfate and evaporated to dryness. Recrystalisation from ether and ethyl acetate at −20° C. yielded a colourless powder (2.8 g, 6.7 mmole, 63.8%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07569225B2uspto-grants-2009_08