反応式
ClC1C=[C:10]2[C:5]([CH2:6][CH2:7][N:8](C3C=NC=CC=3)[C:9]2=O)=[CH:4]C=1.[F:19][C:20]1[CH:21]=[CH:22][C:23]2[S:31][C:30]3[CH2:29][CH2:28][NH:27][C:26](=[O:32])[C:25]=3[C:24]=2[CH:33]=1.IC1C=NC=CC=1C.P([O-])([O-])([O-])=O.[K+].[K+].[K+]>[Cu](I)I.O1CCOCC1>[F:19][C:20]1[CH:21]=[CH:22][C:23]2[S:31][C:30]3[CH2:29][CH2:28][N:27]([C:6]4[CH:7]=[N:8][CH:9]=[CH:10][C:5]=4[CH3:4])[C:26](=[O:32])[C:25]=3[C:24]=2[CH:33]=1参加物
7
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
Using analogous conditions and workup as described for the preparation of Compound 1A, 8-Fluoro-3,4-dihydro-2H-benzo[4,5]thieno[3,2-c]pyridin-1-one (I-50 g: 100 mg, 0.452 mmol) was reacted with 3-iodo-4-methylpyridine (99.09 mg, 0.452 mmol), 1,4-dioxane (5 mL), copper iodide (8.64 mg, 0.0452 mmol), trans-N,N′-dimethyl-cyclohexyl-1,2-diamine (19.25 mg, 0.1356 mmol) and potassium phosphate (287.44 mg, 1.356 mmol) at 115° C. overnight under nitrogen atmosphere to afford the crude product. Purification by column chromatography on silica gel (1.5% methanol in CHCl3) afforded 95 mg of the product (67.37% yield).
後処理
- customto afford the crude product
- customPurification by column chromatography on silica gel (1.5% methanol in CHCl3)
出典と根拠
- ORDレコード
- ord-c3cb0b60a6b047cfba052866f37376d1
- 出典データセット
- uspto-grants-2015_02
- 特許番号
- US08946260B2
関連ノート
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