反応 #2956

ord-ceee2b4669514a49ad828e34aae4470f

反応方程式

CCN1CC[C@]2(c3cccc(OC)c3)CC(=O)CC[C@H]2C1.Cl
(±)-trans-2-ethyl-4a-(3-methoxyphenyl)-6-oxo-1,2,3,4,4a,5,6,7,8,8a-decahydroisoquinoline hydrochloride
CCOC(=O)C(=NNc1ccccc1)C(C)=O
ethyl 2-phenylhydrazono-3-oxobutyrate
CC(=O)[O][Na]
CH3COONa
CCOC(=O)c1[nH]c2c(c1C)C[C@@H]1CN(CC)CC[C@@]1(c1cccc(OC)c1)C2
title compound
収率 61.3%
CCOC(=O)c1[nH]c2c(c1C)C[C@@H]1CN(CC)CC[C@@]1(c1cccc(OC)c1)C2
(±)-trans-6-Ethyl-2-ethoxycarbonyl-3-methyl-8a-(3-methoxyphenyl)-4,4a,5,6,7,8,8a,9-octahydro-1H-pyrrolo[2,3-g]isoquinoline
収率 61.3%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONThe solution was treated
  2. 2
    その他The residue was purified by flash chromatography (AcOEt/MeOH/conc. NH4OH 94:5:0.5; Rf=0.3)

実験手順

0.8 g (2.47 mmol) of (±)-trans-2-ethyl-4a-(3-methoxyphenyl)-6-oxo-1,2,3,4,4a,5,6,7,8,8a-decahydroisoquinoline hydrochloride and 0.87 g (93.7 mmol) of ethyl 2-phenylhydrazono-3-oxobutyrate [Organic Reactions, R. Adams Ed; Wiley, New York, 10, 32-33, (1951-1959)] were dissolved in a mixture of 3 mi of glacial acetic acid and 0.34 g (4.2 mmol) of CH3COONa. The solution was treated as described in example 1 adding 0.74 g (11.3 mmol) of zinc dust. The residue was purified by flash chromatography (AcOEt/MeOH/conc. NH4OH 94:5:0.5; Rf=0.3), obtaining 0.6 g of the title compound.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05731322uspto-grants-1998_03