反応 #2960

ord-a4e872fd5a6e4a58b4e93bf3d6bae84a

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
CCN(CC)C(=O)C(=NNc1ccccc1)C(C)=O
N,N-diethyl-2-phenylhydrazono-3-oxobutyramide
CC(=O)[O][Na]
CH3COONa
CCN(CC)C(=O)c1[nH]c2c(c1C)C[C@@H]1CN(C)CC[C@@]1(c1cccc(OC)c1)C2
title compound
収率 14.7%
CCN(CC)C(=O)c1[nH]c2c(c1C)C[C@@H]1CN(C)CC[C@@]1(c1cccc(OC)c1)C2
(±)-trans-2-Diethylaminocarbonyl-3,6-dimethyl-8a-(3-methoxyphenyl)-4,4a,5,6,7,8,8a,9-octahydro-1H-pyrrolo[2,3-g]isoquinoline
収率 14.7%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The residue was purified by flash chromatography (AcOEt/MeOH/conc. NH4OH 90:10:1; Rf=0.27)

実験手順

3 g (9.3 mmol) of (±)-trans-2-ethyl-4a-(3-methoxyphenyl)-6-oxo-1,2,3,4,4a,5,6,7,8,8a-decahydroisoquinoline hydrochloride, 2.92 g (11.2 mmol) of N,N-diethyl-2-phenylhydrazono-3-oxobutyramide, 0.92 g (11.2 mmol) of CH3COONa, 2.8 g (42.8 mmol) of zinc dust and 9.3 ml of glacial acetic acid were treated as described in example 1. The residue was purified by flash chromatography (AcOEt/MeOH/conc. NH4OH 90:10:1; Rf=0.27) yielding 0.56 g of the title compound. M.p. (.HCl)=250° C. dec. C25H35N3O2I.R. (KBr) (hydrochloride): 3410, 3200, 2915, 2510, 1605, 1580 cm-1.

出典

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