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, 6.153 mmol) in toluene (40 mL) and ethanol (40 mL) was added 4-fluorophenyl boronic acid (1.026 g, 7.384 mmol) and 2 M solution of aqueous Na2CO3. The reaction mixture was degassed with argon, Pd(PPh3)4 (0.354 g, 0.355 mmol) was added, the reaction mixture again degassed with argon for 10 min, and the mixture heated to 100° C. for 2 h. The reaction mixture was evaporated under vacuum to remove the ethanol, diluted with water (50 mL), extracted with ethyl acetate (200 mL), dried over sodium sulfate, filtered and evaporated under reduced pressure to obtain crude product. The crude product was purified by Biotage IsoleraOne® column (using 30% ethyl acetate and hexane) to give (5-(4-fluorophenyl)-1,3,4-thiadiazol-2-yl)methanol as pale yellow solid (0.85 g, 65% yield); LC-MS m/z calculated for [M+H]+ 211.03, found 211.1.
後処理
- additionwas added
- customthe reaction mixture again degassed with argon for 10 min
- customThe reaction mixture was evaporated under vacuum
- customto remove the ethanol
- additiondiluted with water (50 mL)
- extractionextracted with ethyl acetate (200 mL)
- dry with materialdried over sodium sulfate
- filtrationfiltered
- customevaporated under reduced pressure
- customto obtain crude product
- customThe crude product was purified by Biotage IsoleraOne® column (using 30% ethyl acetate and hexane)
出典と根拠
- ORDレコード
- ord-c81ca0e209a64335a060ee8692b6a155
- 出典データセット
- uspto-grants-2014_08
- 特許番号
- US08809372B2
反応ノート
読み込み中…