反応式
[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([C:10]2[C:15]([C:16]([F:19])([F:18])[F:17])=[CH:14][N:13]=[C:12]([O:20]C)[CH:11]=2)[CH:3]=1.Cl.[NH+]1C=CC=CC=1>>[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([C:10]2[C:15]([C:16]([F:17])([F:18])[F:19])=[CH:14][NH:13][C:12](=[O:20])[CH:11]=2)[CH:3]=1参加物
3
実験手順
450 mg (purity 71%, 1.02 mmol) of 4-chloro-2-[2-methoxy-5-(trifluoromethyl)pyridin-4-yl]benzonitrile and 20 eq. of pyridinium hydrochloride were reacted according to General Method 3A. After aqueous work-up, the crude product was purified by flash chromatography (silica gel 60, dichloromethane/methanol mixtures). Yield: 456 mg (purity 86%, quant.)
後処理
- customAfter aqueous work-up, the crude product was purified by flash chromatography (silica gel 60, dichloromethane/methanol mixtures)
出典と根拠
- ORDレコード
- ord-d36814fdac9b4e77a07bdbd443b15151
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09434690B2
関連ノート
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