反応 #5494

ord-37b24b9090dc4d9a9382a6652abf7b0e

反応方程式

CC(=O)SC[C@H]1CCCCCC[C@H](C(=O)O)NC1=O
Trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxylic acid
Nc1cccnc1
3-aminopyridine
On1nnc2ccccc21
1-hydroxybenzotriazole
CN1CCOCC1
4-methylmorpholine
CCN=C=NCCCN(C)C.Cl
N-(dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride
CC(=O)SC[C@H]1CCCCCC[C@H](C(=O)Nc2cccnc2)NC1=O
3-{N-[[trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecan-10-yl]-carbonyl]-amino}-pyridine

反応条件

温度
0°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度to warm up to room temperature
  2. 2
    その他The reaction is partitioned between methylene chloride and water
  3. 3
    乾燥the organic layer is dried (MgSO4)
  4. 4
    その他the solvent is evaporated
  5. 5
    その他The product is purified by silica gel chromatography (70% ethyl acetate/hexane)

実験手順

Trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecane-10-carboxylic acid (0.100 g, 0.35 mmol), 3-aminopyridine (0.036 g, 0.38 mmol), 1-hydroxybenzotriazole (0.047 g, 0.035 mmol), and 4-methylmorpholine (0.077 mL, 0.70 mmol) are dissolved in methylene chloride (2.5 mL), and the reaction is cooled to 0° C. To this solution is added N-(dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (0.134 g, 0.70 mmol), and the reaction is allowed to warm up to room temperature and then stirred overnight. The reaction is partitioned between methylene chloride and water, the organic layer is dried (MgSO4), and the solvent is evaporated. The product is purified by silica gel chromatography (70% ethyl acetate/hexane) to give 3-{N-[[trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecan-10-yl]-carbonyl]-amino}-pyridine, MS: M+1=364.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05244889uspto-grants-1993_09