反応 #2971

ord-53e465a32b0c4c70bcd0b9d12d1a9382

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(=O)N(C)C
N, N-dimethyl-2-phenylhydrazono-3-oxobutyramide
CC(=O)[O][Na]
CH3COONa
Cc1c[nH]c2c1CC1CNCCC1C2
product
収率 84.8%
Cc1c[nH]c2c1CC1CNCCC1C2
3-methyl-4,4a,5,6,7,8,8a,9-octahydro-1H-pyrrolo[2,3-g]isoquinoline
収率 84.8%

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 (EtOAc/MeOH 0%→30%)

実験手順

1.0 g (3.1 mmol) of (±)-trans-2-ethyl-4a-(3-methoxyphenyl)-6-oxo-1,2,3,4,4a,5,6,7,8,8a-decahydroisoquinoline hydrochloride, 2.33 g (10 mmol) of N, N-dimethyl-2-phenylhydrazono-3-oxobutyramide, 0.82 g (1 0 mmol) of CH3COONa, 2.6 g (40 mmol) of zinc dust and 5 ml of glacial acetic acid were treated as described in example 1. The residue was purified by chromatography on silica gel (EtOAc/MeOH 0%→30%) yielding 0.5 g of product which was crystallized from Et2O yielding 0.5 g of the title compound. M.p.=151°-153° C.

出典

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