反応式
[CH3:1][O:2][C:3]1[NH:4][C:5]([CH3:10])=[CH:6][C:7]=1[C:8]#[N:9].[F:11][C:12]([S:15]Cl)([Cl:14])[Cl:13]>C(Cl)Cl>[CH3:1][O:2][C:3]1[NH:4][C:5]([CH3:10])=[C:6]([S:15][C:12]([Cl:14])([Cl:13])[F:11])[C:7]=1[C:8]#[N:9]参加物
4
実験手順
A suspension of 2-methoxy-3-cyano-5-methylpyrrole (0.5 g) in 5 ml of CH2Cl2 was treated with Cl2FCSCl (0.45 ml) and stirred at room temperature for 14 h. The resulting precipitate was filtered, washed with CH2Cl2, and dried under high vacuum to afford an off-white solid (0.59 g), m.p. 175° C.
後処理
- filtrationThe resulting precipitate was filtered
- washwashed with CH2Cl2
- customdried under high vacuum
出典と根拠
- ORDレコード
- ord-af276a2a619b4f6bbb7ebd9628e774c3
- 出典データセット
- uspto-grants-2001_08
- 特許番号
- US06271392B1
関連ノート
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