反応式
[Cl:1][C:2]1[C:3]([C:10]2[CH:15]=[C:14]([Cl:16])[CH:13]=[CH:12][C:11]=2[CH:17]([F:19])[F:18])=[CH:4][C:5]([O:8]C)=[N:6][CH:7]=1.[Cl-].[NH+]1C=CC=CC=1>>[Cl:1][C:2]1[C:3]([C:10]2[CH:15]=[C:14]([Cl:16])[CH:13]=[CH:12][C:11]=2[CH:17]([F:19])[F:18])=[CH:4][C:5](=[O:8])[NH:6][CH:7]=1参加物
3
実験手順
305 mg (purity 77%, 0.77 mmol) of 5-chloro-4-[5-chloro-2-(difluoromethyl)phenyl]-2-methoxypyridine and 20 eq. of pyridinium chloride were reacted according to General Method 3A. After work-up, the crude product was purified by preparative HPLC (Reprosil C18, water/acetonitrile gradient). Yield: 179 mg (80% of theory)
後処理
- customAfter work-up, the crude product was purified by preparative HPLC (Reprosil C18, water/acetonitrile gradient)
出典と根拠
- ORDレコード
- ord-b098b5f42e87484490369782a0a6d1f2
- 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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