Potassium Phosphate, Tribasic → HCID 178466665、化合物
反応式
[F:1][C:2]1[CH:23]=[C:22]([F:24])[CH:21]=[CH:20][C:3]=1[O:4][C:5]1[N:10]=[C:9]2[NH:11][N:12]=[CH:13][C:8]2=[C:7]([NH:14][CH2:15][CH:16]([OH:19])[CH2:17]I)[N:6]=1.[F:25][C:26]1[CH:27]=[CH:28][C:29]([O:35][CH2:36][CH3:37])=[C:30](B(O)O)[CH:31]=1.[O-]P([O-])([O-])=O.[K+].[K+].[K+]>O1CCOCC1>[F:1][C:2]1[CH:23]=[C:22]([F:24])[CH:21]=[CH:20][C:3]=1[O:4][C:5]1[N:10]=[C:9]2[NH:11][N:12]=[C:13]([C:28]3[CH:27]=[C:26]([F:25])[CH:31]=[CH:30][C:29]=3[O:35][CH2:36][CH3:37])[C:8]2=[C:7]([NH:14][CH2:15][C@H:16]([OH:19])[CH3:17])[N:6]=1参加物
反応条件
- 温度
- 180 °C
実験手順
1-[6-(2,4-Difluoro-phenoxy)-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-ylamino-propan-2-ol (200 mg, 0.447 mmol), 5-fluoro-2-ethoxyphenyl boronic acid (246 mg), K3PO4 (285 mg), and Tetrakis(triphenylphosphine) palladium(0) CH2Cl2 (73 mg) were added to 2 mL dioxane in a microwave vial. The vial was sealed and the reaction mixture was heated to 180° C. for 10 minutes. The reaction mixture was partitioned between water and ethyl acetate, and the organic layer was separated, dried over MgSO4, filtered, and evaporated under reduced pressure. The residue was filtered through silica gel using 10% MeOH in methylene chloride, then purified by preparative scale thin layer chromatography using 10% MeOH in methylene chloride, to give 62.9 mg of (R)-1-[6-(2,4-Difluoro-phenoxy)-3-(2-ethoxy-5-fluoro-phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-ylamino]-propan-2-ol. Mass Spec. M+H=460.
後処理
- customThe vial was sealed
- customThe reaction mixture was partitioned between water and ethyl acetate
- customthe organic layer was separated
- dry with materialdried over MgSO4
- filtrationfiltered
- customevaporated under reduced pressure
- filtrationThe residue was filtered through silica gel using 10% MeOH in methylene chloride
- custompurified by preparative scale thin layer chromatography
出典と根拠
- ORDレコード
- ord-3ca40e5d5348429f8408ee7b71877e88
- 出典データセット
- uspto-grants-2008_10
- 特許番号
- US07435731B2
反応ノート
読み込み中…