1,8-Diazabicyclo(5.4.0)undec-7-ene → 6-Bromo-4-fluoro-1-benzothiophene
反応式
[Br:1][C:2]1[CH:3]=[C:4]([F:14])[C:5]2[CH:9]=[C:8](C(O)=O)[S:7][C:6]=2[CH:13]=1.C1CCN2C(=NCCC2)CC1>CC(N(C)C)=O>[Br:1][C:2]1[CH:3]=[C:4]([F:14])[C:5]2[CH:9]=[CH:8][S:7][C:6]=2[CH:13]=1参加物
4
実験手順
Using analogous reaction condition and reagents as described in Example 25 for the preparation of I-25c above, 6-bromo-4-fluoro-benzo[b]thiophene-2-carboxylic acid (I-26c: 1.8 g, 6.47 mmol) in DMA (4 mL) and DBU (4.0 g, 26.54 mmol) were heated in microwave to afford the crude product. Purification by column chromatography on silica gel (100% hexane) afforded 1.45 g of the product (97% yield).
後処理
- temperaturewere heated in microwave
- customto afford the crude product
- customPurification by column chromatography on silica gel (100% hexane)
出典と根拠
- ORDレコード
- ord-9cbb22901b2f4732bb9e45a1a5b58a4d
- 出典データセット
- uspto-grants-2015_05
- 特許番号
- US09029399B2
反応ノート
読み込み中…