Trityl chloride → 3-Bromo-4-fluoro-1-trityl-1H-indazole-5-carboxylic Acid Methyl Ester

HRID 1610141ノート

反応式

HRID 1610141 の反応式
[CH3:1][O:2][C:3]([C:5]1[C:6]([F:15])=[C:7]2[C:11](=[CH:12][CH:13]=1)[NH:10][N:9]=[C:8]2[Br:14])=[O:4].[H-].[Na+].[C:18]1([C:24](Cl)([C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)[C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1.C(=O)([O-])O.[Na+]>O1CCCC1>[CH3:1][O:2][C:3]([C:5]1[C:6]([F:15])=[C:7]2[C:11](=[CH:12][CH:13]=1)[N:10]([C:24]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)([C:31]1[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=1)[C:25]1[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=1)[N:9]=[C:8]2[Br:14])=[O:4]

参加物

6

反応物 4

HCID 6456Trityl chlorideHCID 24758Sodium hydrideHCID 516892Sodium BicarbonateHCID 178497388HCID 178497388、化合物

生成物 1

HCID 684205673-Bromo-4-fluoro-1-trityl-1H-indazole-5-carboxylic Acid Methyl Ester収率 30.7%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

Under ice-cooling, to a solution of 2.99 g of 3-bromo-4-fluoro-1H-5-indazolecarboxylic acid methyl ester obtained in Production Example II-13-d in 30 ml tetrahydrofuran was added 526 mg of 60% sodium hydride, and the mixture was stirred for 25 minutes. Then, 3.21 g of triphenylmethyl chloride was added and the mixture was stirred at the same temperature for 15 minutes and further stirred at room temperature for 45 minutes. The reaction mixture was ice-cooled again, saturated aqueous sodium hydrogencarbonate solution was added and the mixture was extracted with 100 ml of ethyl acetate. The organic layer was sequentially washed with water (×2) and brine, dried over anhydrous magnesium sulfate and the solvent was evaporated. The crude product was purified and separated by silica gel column chromatography (ethyl acetate:hexane=1:9), and the resulting crystals were recrystallized from diisopropyl ether, to give 1.73 g of the title compound as white needles.

後処理

  1. stirringthe mixture was stirred at the same temperature for 15 minutes
  2. stirringfurther stirred at room temperature for 45 minutes
  3. temperaturecooled again
  4. extractionthe mixture was extracted with 100 ml of ethyl acetate
  5. washThe organic layer was sequentially washed with water (×2) and brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customthe solvent was evaporated
  8. customThe crude product was purified
  9. customseparated by silica gel column chromatography (ethyl acetate:hexane=1:9)
  10. customthe resulting crystals were recrystallized from diisopropyl ether

出典と根拠

ORDレコード
ord-d1fe7504380644fe80a0d28046373c52
出典データセット
uspto-grants-2006_01
特許番号
US06982274B2

反応ノート

読み込み中…