Reacción #5496

ord-78b42a7c2bd74f04a8c7a9f150514491

Ecuación de reacción

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

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

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

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05244889uspto-grants-1993_09