反応 #46592

ord-e848bcc541084c97af96ce82d283157e

反応方程式

O=C1CCc2cc(Br)cnc2N1
6-bromo-3,4-dihydro-1H-1,8-naphthyridin-2-one
C=CC(=O)OCC
ethyl acrylate
Cc1ccccc1P(c1ccccc1C)c1ccccc1C
tri-ortho-tolylphosphine
CCN(C(C)C)C(C)C
diisopropylethylamine
CCOC(=O)/C=C/c1cnc2c(c1)CCC(=O)N2
title compound
収率 59.0%
CCOC(=O)/C=C/c1cnc2c(c1)CCC(=O)N2
Ethyl (E)-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)acrylate
収率 59.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度was heated
  2. 2
    温度at reflux overnight
  3. 3
    ろ過The dark mixture was filtered through Celite®
  4. 4
    濃縮the filtrate was concentrated

実験手順

A solution of 6-bromo-3,4-dihydro-1H-1,8-naphthyridin-2-one (5.0 g, 21.9 mmole), from Preparation 4, ethyl acrylate (3.3 g, 32.9 mmole), Pd(OAc)2 (1.1 g, 0.74 mmole), tri-ortho-tolylphosphine (1.3 g, 4.4 mmole), and diisopropylethylamine (11.4 mL, 65.7 mmole) in propionitrile (200 mL) and DMF (25 mL) was heated at reflux overnight. The dark mixture was filtered through Celite®, and the filtrate was concentrated. Flash chromatography on silica gel (9:1 CHCl3/CH3OH containing 5% NH4OH) gave the title compound (3.0 g, 59%) as a light yellow solid: MS (ES) m/e 233 (M+H)+.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07741339B2uspto-grants-2010_06