تفاعل #5496

ord-78b42a7c2bd74f04a8c7a9f150514491

معادلة التفاعل

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

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةto warm up to room temperature
  2. 2
    غسيلthe organic layer is washed with 1N hydrochloric acid, saturated sodium bicarbonate
  3. 3
    تجفيفdried (MgSO4)
  4. 4
    أخرىthe solvent is evaporated
  5. 5
    أخرىThe product is purified by silica gel chromatography (75% ethyl acetate/hexane)

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05244889uspto-grants-1993_09