반응 #46592

ord-e848bcc541084c97af96ce82d283157e

반응 방정식

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
수율 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
수율 59.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도was heated
  2. 2
    온도at reflux overnight
  3. 3
    여과The dark mixture was filtered through Celite®
  4. 4
    농축the filtrate was concentrated

실험 절차

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)+.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07741339B2uspto-grants-2010_06