反応 #2969

ord-d4dc502d78a2417cbeb0d77e8113c760

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
CC(=O)C(=NNc1ccccc1)C(N)=O
2-phenylhydrazono-3-oxobutyramide
CC(=O)[O][Na]
CH3COONa
CC(=O)O
acetic acid
CCN1CC[C@@]2(c3cccc(OC)c3)Cc3[nH]c(C(N)=O)c(C)c3C[C@@H]2C1
oily product
CCN1CC[C@@]2(c3cccc(OC)c3)Cc3[nH]c(C(N)=O)c(C)c3C[C@@H]2C1
(±)-trans-2-Aminocarbonyl-6-ethyl-8a-(3-methoxyphenyl)-3-methyl-4,4a,5,6,7,8,8a,9-octahydro-1H-pyrrolo[2,3-g]isoquinoline

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 chromatography on silica gel (Et2O-EtOAc/MeOH 0%→50%)

実験手順

3.24 g (10 mmol) of (±)-trans-2-ethyl-4a-(3-methoxyphenyl)-6-oxo-1,2,3,4,4a,5,6,7,8,8a-decahydroisoquinoline hydrochloride, 6.16 g (30.0 mmol) of 2-phenylhydrazono-3-oxobutyramide, 2.46 g (7.0 mmol) of CH3COONa, 7.85 g (120.0 mmol) of zinc dust and 15 ml of glacial acetic acid were treated as described in example 1. The residue was purified by chromatography on silica gel (Et2O-EtOAc/MeOH 0%→50%) yielding 3.0 g of oily product which was triturated in Et2O yielding 2.5 g of the title compound. M.p.=176°-178° C.

出典

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