反応式
[CH:1]([NH:3][CH2:4][CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)=[O:2].[C:12](Br)(=[O:14])[CH3:13].[Cl-].[Al+3].[Cl-].[Cl-]>ClCCCl>[CH:1]([NH:3][CH2:4][CH2:5][C:6]1[CH:11]=[CH:10][C:9]([C:12](=[O:14])[CH3:13])=[CH:8][CH:7]=1)=[O:2]参加物
5
実験手順
This was prepared in an identical manner to the compound described in Description 10 using N-formyl-2-phenylethanamine (95 g), acetylbromide (128 ml), aluminium chloride (288 g) in 1,2-dichloroethane (900 ml). 25 g of the crude produce was chromatographed on Kieselgel 60 (1 Kg). Elution with 1% methanol-chloroform gave the title compound as an oil (18 g). τ(CDCl3) 7.42 (3H, s), 7.1 (2H, t, J=7 Hz), 6.5 (2H, m), 3.45 (1H, broad), 2.7 (2H, d, J=8 Hz) 2.1 (2H, d, J=8 Hz), 1.9 (1H, s).
後処理
- customThis was prepared in an identical manner to the compound
- custom25 g of the crude produce
- customwas chromatographed on Kieselgel 60 (1 Kg)
- washElution with 1% methanol-chloroform
出典と根拠
- ORDレコード
- ord-433aaae29f2a45c1bf0099ec91d1387e
- 出典データセット
- uspto-grants-1982_01
- 特許番号
- US04309443
関連ノート
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