反応 #169679

ord-fc896c23da2242d7900eafd518759ae6

反応方程式

O=C(O)c1cccnc1
niacin
CN1CCOCC1
N-methyl morpholine
COC(=O)[C@@H](N)CC(C)C.Cl
L-leucinemethyl ester hydrochloride
COC(=O)C(N)(CC(C)C)C(=O)c1cccnc1
required product
収率 72.6%
COC(=O)C(N)(CC(C)C)C(=O)c1cccnc1
4-methyl-2-[pyridine-3-carbonyl]-amino-pentanoic acid methyl ester
収率 72.6%

溶媒

反応条件

温度
25°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    洗浄washed with water (3×100 mL)
  2. 2
    乾燥dried over sodium sulphate
  3. 3
    その他The crude product obtained upon evaporation of the solvent
  4. 4
    その他was further purified by silica gel column chromatography

実験手順

To a solution of niacin (1.35 g, 11.0 mmol) in DCM (20 mL) were added N-methyl morpholine (3.34 g, 33.00 mmol) EDCI.HCl (4.2 g, 22.02 mmol), and L-leucinemethyl ester hydrochloride (2.0 g, 11.0 mmol). The mixture was allowed to stir at room temperature (25° C.) over 2.5 h under nitrogen atmosphere. The resulting mixture was diluted with DCM (200 mL), washed with water (3×100 mL) and dried over sodium sulphate. The crude product obtained upon evaporation of the solvent was further purified by silica gel column chromatography to obtain required product as white solid (2.0 g, 72%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08846721B2uspto-grants-2014_09