反応 #1687630

ord-a6c4d50c601d4a1d9e0335176c247146

反応方程式

O=C(O)c1cccnc1
nicotinic acid
COC(=O)CN.Cl
methyl glycinate hydrochloride
C(=NC1CCCCC1)=NC1CCCCC1
dicyclohexylcarbodiimide
Cc1ccc(S(=O)(=O)O)cc1
p-toluenesulfonic acid
COC(=O)CNC(=O)c1cccnc1
77
COC(=O)CNC(=O)c1cccnc1
N-Methoxycarbonylmethyl-nicotinamide

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過Filtration and evaporation in vacuo
  2. 2
    その他gave a heavy oil which
  3. 3
    抽出After basification with ammonia the aqueous solution was extracted with 3×300 ml of dichloromethane
  4. 4
    乾燥The organic phase was dried over magnesium sulphate, and removal of the solvent in vacuo

実験手順

A mixture of 50.0 g (0.400 mol) of nicotinic acid, 50.0 g (0.400 mol) of methyl glycinate hydrochloride, 90 g (0.440 mol) of dicyclohexylcarbodiimide, and 2 g of p-toluenesulfonic acid in 500 ml of dry pyridine was stirred overnight at room temperature. Filtration and evaporation in vacuo gave a heavy oil which was dissolved in 500 ml of water. After basification with ammonia the aqueous solution was extracted with 3×300 ml of dichloromethane. The organic phase was dried over magnesium sulphate, and removal of the solvent in vacuo gave crude 77 as a heavy yellow oil. Yield: 63.0 g (0.320 mol, 81%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: USRE036374uspto-grants-1999_11