Reaktion #50250

ord-7951d5471ad442c6af52215ba75dbe41

Reaktionsgleichung

CC(=O)SC[C@H]1CCCCCC[C@H](C(=O)O)NC1=O
Trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxylic acid
CC(=O)OCCN.Cl
1-acetoxy-2-aminoethane hydrochloride
On1nnc2ccccc21
1-hydroxybenzotriazole
CN1CCOCC1
4-methylmorpholine
CCN=C=NCCCN(C)C.Cl
N-(dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride
CC(=O)OCCNC(=O)[C@H]1CCCCCC[C@H](CSC(C)=O)C(=O)N1
2-acetoxy-N-[[trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecan-10-yl]-carbonyl]-ethylamine

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturto warm up to room temperature
  2. 2
    Waschenthe organic layer is washed with 1N hydrochloric acid, saturated sodium bicarbonate
  3. 3
    Trocknendried (MgSO4)
  4. 4
    Sonstigethe solvent is evaporated
  5. 5
    SonstigeThe product is purified by silica gel chromatography (75% ethyl acetate/hexane)

Vorschrift

Trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxylic acid (0.15 g, 0.52 mmol), 1-acetoxy-2-aminoethane hydrochloride (0.073 g, 0.52 mmol), 1-hydroxybenzotriazole (0.12 g, 0.52 mmol), and 4-methylmorpholine (0.17 mL, 1.56 mmol) are dissolved in methylene chloride (3.0 mL), and the reaction is cooled to 0° C. To this solution is added N-(dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (0.20 g, 1.04 mmol), and the reaction is allowed to warm up to room temperature and then stirred overnight. The reaction is diluted with more methylene chloride, and the organic layer is washed with 1N hydrochloric acid, saturated sodium bicarbonate, dried (MgSO4), and the solvent is evaporated. The product is purified by silica gel chromatography (75% ethyl acetate/hexane) to give 2-acetoxy-N-[[trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecan-10-yl]-carbonyl]-ethylamine, MS: M+1=373.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05426103uspto-grants-1995_06