反応式
[F:1][C:2]1([F:26])[CH2:7][CH2:6][N:5]([C:8]([C:10]2[NH:11][C:12]3[C:17]([CH:18]=2)=[CH:16][C:15]([O:19][CH:20]2[CH2:25][CH2:24][NH:23][CH2:22][CH2:21]2)=[CH:14][CH:13]=3)=[O:9])[CH2:4][CH2:3]1.C(O)(=O)C.[C:31]1(=O)[CH2:34][CH2:33][CH2:32]1.C(O[BH3-])(=O)C.[Na+]>O1CCCC1.O.C(OCC)(=O)C>[CH:31]1([N:23]2[CH2:24][CH2:25][CH:20]([O:19][C:15]3[CH:16]=[C:17]4[C:12](=[CH:13][CH:14]=3)[NH:11][C:10]([C:8]([N:5]3[CH2:6][CH2:7][C:2]([F:1])([F:26])[CH2:3][CH2:4]3)=[O:9])=[CH:18]4)[CH2:21][CH2:22]2)[CH2:34][CH2:33][CH2:32]1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 3
反応条件
- 温度
- 55 °C
実験手順
A mixture of (4,4-difluoro-piperidin-1-yl)-[5-(piperidin-4-yloxy)-1H-indol-2-yl]-methanone (example 43, step 6, 350 mg, 1.0 eq.), acetic acid (0.17 mL, 3.0 eq.) and cyclobutanone (138 mg, 2.0 eq.) in tetrahydrofuran (6 mL) was stirred at 55° C. for 1 h. At room temperature, sodium acetoxyborohydride (421 mg, 2.0 eq.) was added and the mixture stirred for 16 h at 65° C. The reaction mixture was partitionned between ethyl acetate and water. The aqueous layer was extracted twice with ethyl acetate and the combined organic fractions were washed twice with saturated sodium bicarbonate solution, dried over sodium sulfate, filtered, evaporated to dryness and purified on silica gel, eluting with a 49:1:0 to 95:5:0.25 gradient of dichloromethane/methanol/ammonium hydroxide, to yield 265 mg (65%) from the desired product as off-white solid. MS (m/e): 418.1 (MH+, 100%).
後処理
- stirringthe mixture stirred for 16 h at 65° C
- extractionThe aqueous layer was extracted twice with ethyl acetate
- washthe combined organic fractions were washed twice with saturated sodium bicarbonate solution
- dry with materialdried over sodium sulfate
- filtrationfiltered
- customevaporated to dryness
- custompurified on silica gel
- washeluting with a 49:1:0 to 95:5:0.25 gradient of dichloromethane/methanol/ammonium hydroxide
出典と根拠
- ORDレコード
- ord-dacabf58836542c1aa82874a9bbf70eb
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07745479B2
関連ノート
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