反応 #2963

ord-4a987530b45942d59d9beddfbfacbbc6

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)NCc1ccccc1
N-benzyl-2-phenylhydrazono-3-oxobutyramide
COc1cccc([C@@]23CCN(C)C[C@H]2Cc2c([nH]c(C(=O)NCc4ccccc4)c2C)C3)c1
(±)-trans-2-Benzylaminocarbonyl-3,6-dimethyl-8a-(3-methoxyphenyl)-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 crystallised from AcOEt yielding 0.65 g of the title compound

実験手順

1 g (3.3 mmol) of (±)-trans-2-ethyl-4a-(3-methoxyphenyl)-6-oxo-1,2,3,4,4a,5,6,7,8,8a-decahydroisoquinoline hydrochloride, 2.95 g (10 mmol) of N-benzyl-2-phenylhydrazono-3-oxobutyramide, 0.82 g (10 mmol) of CH3 COONa, 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 crystallised from AcOEt yielding 0.65 g of the title compound. M. p.=162°-164° C.

出典

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