Water → HCID 86698767、化合物
反応式
Br[C:2]1[CH:13]=[CH:12][C:5]2[O:6][C@H:7]([CH2:10][OH:11])[CH2:8][O:9][C:4]=2[CH:3]=1.[Cl:14][C:15]1[CH:23]=[C:22]2[C:18]([CH:19]=[CH:20][NH:21]2)=[CH:17][C:16]=1B1OCC(C)(C)CO1.[C:32](=O)([O-])[O-:33].[K+].[K+].O>CN(C=O)C.O1CCOCC1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].C(Cl)Cl>[Cl:14][C:15]1[CH:23]=[C:22]2[C:18]([C:19]([CH:32]=[O:33])=[CH:20][NH:21]2)=[CH:17][C:16]=1[C:2]1[CH:13]=[CH:12][C:5]2[O:6][C@H:7]([CH2:10][OH:11])[CH2:8][O:9][C:4]=2[CH:3]=1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 4
実験手順
A mixture of [(2R)-6-bromo-2,3-dihydro-1,4-benzodioxin-2-yl]methanol (0.54 g, 2.05 mmol) (which can be prepared as in Biorg. Med. Chem. 2007, 15, 4048.), 6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indole (0.52 g, 4.06 mmol) in DMF (4 mL) and dioxane (4 mL) was stirred at room temperature for 30 min. under N2. Pd(dppf)Cl2 (100 mg, 0.137 mmol) and 2N potassium carbonate (10 mL, 20 mmol) was added. The resulting mixture was stirred for 30 min. at 90° C. under N2. TLC showed the reaction was complete. Water (50 mL) and methylene chloride (50 mL) was added. The aqueous layer was extracted with methylene chloride (30 mL×3). The combined organic layer was dried over sodium sulfate, filtered and evaporated to give the title compound (1 g) which was used in the next step without further purification.
後処理
- stirringThe resulting mixture was stirred for 30 min. at 90° C. under N2
- extractionThe aqueous layer was extracted with methylene chloride (30 mL×3)
- dry with materialThe combined organic layer was dried over sodium sulfate
- filtrationfiltered
- customevaporated
出典と根拠
- ORDレコード
- ord-4ca624900ee84a59a60d91bc6285783f
- 出典データセット
- uspto-grants-2014_11
- 特許番号
- US08889730B2
反応ノート
読み込み中…