Sodium Carbonate → HCID 57598244、化合物
反応式
Br[C:2]1[S:6][C:5]([CH2:7][OH:8])=[N:4][N:3]=1.[F:9][C:10]1[CH:15]=[CH:14][C:13](B(O)O)=[CH:12][CH:11]=1.C([O-])([O-])=O.[Na+].[Na+]>C1(C)C=CC=CC=1.C(O)C.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[F:9][C:10]1[CH:15]=[CH:14][C:13]([C:2]2[S:6][C:5]([CH2:7][OH:8])=[N:4][N:3]=2)=[CH:12][CH:11]=1参加物
反応条件
- 温度
- 100 °C
実験手順
To a solution of (5-bromo-1,3,4-thiadiazol-2-yl)methanol (1.2 g, 6.15 mmol) in toluene (40 ml) and ethanol (40 ml) was added 4-fluorophenyl boronic acid (1.03 g, 7.38 mmol) and 2 M aqueous Na2CO3. The reaction mixture was degassed with argon, Pd(PPh3)4 (0.354 g, 0.355 mmol) was added, the reaction mixture was degassed again with argon for 10 min, and then heated to 100° C. for 2 h. The reaction mixture was evaporated under vacuum to remove ethanol, the reaction mixture was diluted with water (50 mL), and extracted with ethyl acetate (200 mL). The organic extracts were dried over sodium sulphate, filtered and evaporated under reduced pressure to obtain crude product. The crude product was purified by Biotage Isolera® One column (using 30% ethyl acetate and hexane) to give (5-(4-fluorophenyl)-1,3,4-thiadiazol-2-yl)methanol as a pale yellow solid (0.85 g, 65% yield); LC-MS m/z calcd for [M+H]+ 211.03. found 211.1
後処理
- additionwas added
- customthe reaction mixture was degassed again with argon for 10 min
- customThe reaction mixture was evaporated under vacuum
- customto remove ethanol
- additionthe reaction mixture was diluted with water (50 mL)
- extractionextracted with ethyl acetate (200 mL)
- dry with materialThe organic extracts were dried over sodium sulphate
- filtrationfiltered
- customevaporated under reduced pressure
- customto obtain crude product
- customThe crude product was purified by Biotage Isolera® One column (using 30% ethyl acetate and hexane)
出典と根拠
- ORDレコード
- ord-b6077b0dca584e63b901f539d10d6337
- 出典データセット
- uspto-grants-2015_12
- 特許番号
- US09199975B2
反応ノート
読み込み中…