反応式
Br[C:2]1[S:3][CH:4]=[C:5]([Br:7])[CH:6]=1.[Cl:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]2[CH:16]=[CH:17][C:18]([C:21]#[CH:22])=[N:19][CH:20]=2)=[CH:11][CH:10]=1.BrCl>>[Br:7][C:5]1[CH:6]=[C:2]([C:22]#[C:21][C:18]2[CH:17]=[CH:16][C:15]([C:12]3[CH:13]=[CH:14][C:9]([Cl:8])=[CH:10][CH:11]=3)=[CH:20][N:19]=2)[S:3][CH:4]=1参加物
4
実験手順
The product was obtained analogously to Example 7.1e starting from 2,4-dibromothiophene and 5-(4-chlorophenyl)-2-ethynylpyridine. Yield: 0.78 g (50% of theoretical); C17H9BrClNS (M=374.683); calc.: molpeak (M+H)+: 374/376/378 (BrCl); found: molpeak (M+H)+: 374/376/378 (BrCl); HPLC-MS: 7.40 minutes (method B).
後処理
- customThe product was obtained analogously to Example 7.1e
- custom7.40 minutes (method B)
出典と根拠
- ORDレコード
- ord-2a6c6e1e5fbe45b59a49c621ac3ab274
- 出典データセット
- uspto-grants-2009_09
- 特許番号
- US07592358B2
関連ノート
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