Potassium Carbonate → HCID 59199313、化合物
反応式
Br[C:2]1[CH:3]=[C:4]([C:23]([F:26])([F:25])[F:24])[CH:5]=[C:6]2[C:11]=1[N:10]=[C:9]([NH:12][C:13]1[CH:18]=[CH:17][C:16]([S:19]([NH2:22])(=[O:21])=[O:20])=[CH:15][CH:14]=1)[N:8]=[CH:7]2.[F:27][C:28]1[CH:33]=[CH:32][C:31](B(O)O)=[CH:30][N:29]=1.C(=O)([O-])[O-].[K+].[K+]>COCCOC.C(OCC)(=O)C>[F:27][C:28]1[N:29]=[CH:30][C:31]([C:2]2[CH:3]=[C:4]([C:23]([F:26])([F:24])[F:25])[CH:5]=[C:6]3[C:11]=2[N:10]=[C:9]([NH:12][C:13]2[CH:14]=[CH:15][C:16]([S:19]([NH2:22])(=[O:21])=[O:20])=[CH:17][CH:18]=2)[N:8]=[CH:7]3)=[CH:32][CH:33]=1参加物
6
実験手順
To a 0.050 M solution of 4-(8-bromo-6-(trifluoromethyl)quinazolin-2-ylamino)benzenesulfonamide (1.0 eq) in DME was added 2-fluoro-5-pyridineboronic acid (3.0 eq), (dppf)Pd(II)Cl2-CH2Cl2 (0.050 eq) and 2M aqueous potassium carbonate (8.0 eq). The mixture was microwaved at 120° C. for 10 min and then diluted with ethyl acetate and filtered through a pad of silica gel. The filtrate was concentrated to give the desired product which was used without further purification. ES/MS m/z 464 (MH+).
後処理
- customThe mixture was microwaved at 120° C. for 10 min
- filtrationfiltered through a pad of silica gel
- concentrationThe filtrate was concentrated
出典と根拠
- ORDレコード
- ord-8d40c7a4fba04c7db3b326dacee65c9c
- 出典データセット
- uspto-grants-2011_04
- 特許番号
- US07932262B2
反応ノート
読み込み中…