반응 #42003

ord-5ddb13722ece4107bca665ef961a4d5b

반응 방정식

CCCCCCCCCCCC(=O)N[C@H](C(=O)O)C(C)C
N-lauroyl-L-valine
O.O=C1CCC(=O)N1O
N-hydroxysuccinimide monohydrate
ClC(Cl)Cl
chloroform
NC1CCCCC1
cyclohexylamine
CCCCCCCCCCCC(=O)N[C@H](C(=O)NC1CCCCC1)C(C)C
N-lauroyl-L-valine cyclohexylamide
수율 44.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척washed with 25 mL of 0.2N hydrochloric acid, 20 mL of water and 20 mL of a saturated aqueous solution of sodium hydrogen carbonate
  2. 2
    건조The mixture was then dried with anhydrous sodium sulfate and condensed under reduced pressure
  3. 3
    기타The residue was purified with a thin-layer chromatography (silica gel, chloroform:methanol=20:1)

실험 절차

61 mg (0.20 mmol) of N-lauroyl-L-valine and 39 mg (0.26 mmol) of N-hydroxysuccinimide monohydrate were dissolved into 3.0 mL of dried chloroform. 50 mg (0.26 mmol) of 1-ethyl-3-(3-dimethylpropyl)carbodiimide hydrochloride was added thereto under argon atmosphere and in the ice bath, and stirred at 0° C. for 3 hours. 35 μL of triethylamine and 35 μL of cyclohexylamine were added thereto and stirred at room temperature overnight. Then, 20 mL of ethyl acetate was added thereto and washed with 25 mL of 0.2N hydrochloric acid, 20 mL of water and 20 mL of a saturated aqueous solution of sodium hydrogen carbonate. The mixture was then dried with anhydrous sodium sulfate and condensed under reduced pressure. The residue was purified with a thin-layer chromatography (silica gel, chloroform:methanol=20:1) to obtain 34 mg of N-lauroyl-L-valine cyclohexylamide (0.089 mmol, yield 44%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07728158B2uspto-grants-2010_06