Réaction #470380

ord-3c987f56724b4e878d2713b95c2e3c80

Équation de réaction

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
Rendement 63.8%
O=C(N[C@@H](CSCC(O)CO)C(=O)O)OCc1cccc2c1Cc1ccccc1-2
N-Fluorenylmethoxycarbonyl-S-(2,3-dihydroxypropyl)cysteine
Rendement 63.8%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Extractionextracted with diethyl ether (25 ml×3)
  2. 2
    Extractionwas then extracted with ethyl acetate (70 ml×3)
  3. 3
    LavageThe extract was washed with water (50 ml×2) and saturated sodium chloride solution (50 ml×2)
  4. 4
    Séchagedried over sodium sulfate
  5. 5
    Autreevaporated to dryness
  6. 6
    AutreRecrystallisation from ether and ethyl acetate at −20° C.

Mode opératoire

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. Recrystallisation from ether and ethyl acetate at −20° C. yielded a colourless powder (2.8 g, 6.7 mmole, 63.8%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08367067B2uspto-grants-2013_02