反応式
Br[CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:7]=[C:8]([C:12]2[C:16]3[S:17][CH:18]=[CH:19][C:15]=3[O:14][N:13]=2)[CH:9]=[CH:10][CH:11]=1.ClCCCOC1C=C([C:31]2[C:35]3[S:36][CH:37]=[CH:38][C:34]=3O[N:32]=2)C=CC=1.S1C=CC=C1CN.C(=O)([O-])[O-].[K+].[K+]>>[O:14]1[C:15]2[CH:19]=[CH:18][S:17][C:16]=2[C:12]([C:8]2[CH:7]=[C:6]([CH:11]=[CH:10][CH:9]=2)[O:5][CH2:4][CH2:3][CH2:2][NH:32][CH2:31][C:35]2[S:36][CH:37]=[CH:38][CH:34]=2)=[N:13]1参加物
5
実験手順
The title compound is prepared from a mixture of 3-[3-(3-bromo-propoxy)-phenyl]-thieno[2,3-d]isoxazole, 3-[3-(3-chloro-propoxy)-phenyl]-thieno[2,3-d]isoxazole, 2-thiophenemethylamine and potassium carbonate essentially as described above in example 4. Combine the appropriate fractions and concentrate to give the title compound (0.35 g, 94% Yield) as an oil. Purity by LC/MS (APCI)=100% area, [M+H]+=371 m/e.
後処理
- concentrationCombine the appropriate fractions and concentrate
出典と根拠
- ORDレコード
- ord-6bb6ce2fe8a0479ca1d5204a25a71496
- 出典データセット
- uspto-grants-2006_08
- 特許番号
- US07091199B1
関連ノート
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