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Water → HCID 135910362、化合物

HRID 2423102
ノート
印刷プレビュー

反応式

HRID 2423102 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([OH:26])[C:5]2[CH:6]=[N:7][N:8]([C:11]3[CH:16]=[CH:15][C:14]([O:17]CC4C=CC=CC=4)=[C:13]([F:25])[CH:12]=3)[C:9]=2[CH:10]=1.B(Br)(Br)Br.O.C([O-])(O)=O.[Na+]>C(Cl)Cl>[Cl:1][C:2]1[CH:3]=[C:4]([OH:26])[C:5]2[CH:6]=[N:7][N:8]([C:11]3[CH:16]=[CH:15][C:14]([OH:17])=[C:13]([F:25])[CH:12]=3)[C:9]=2[CH:10]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 25134Boron tribromideHCID 516892Sodium BicarbonateHCID 136085248HCID 136085248、化合物

生成物 1

HCID 135910362HCID 135910362、化合物収率 77.1%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
-78 °C

実験手順

To a suspension of 6-chloro-1-{3-fluoro-4-[(phenylmethyl)oxy]phenyl}-1H-indazol-4-ol (D11) (60 mg, 0.163 mmol) in dry DCM (2 mL) cooled to −78° C. was added BBr3 (1M in DCM, 0.326 mL, 0.326 mmol) dropwise. The resulting mixture was stirred at this temperature for 1 hour, then it was warmed to room temperature, treated with water and the pH adjusted to 7 by addition of saturated NaHCO3. The solution was extracted with EtOAc (2×) and the combined organics were dried over MgSO4. The crude material (49 mg) was then purified by flash chromatography with a gradient of 5-100% EtOAc in hexane to give a the title compound (E8) as a colourless solid (35 mg).

後処理

  1. temperatureit was warmed to room temperature
  2. extractionThe solution was extracted with EtOAc (2×)
  3. dry with materialthe combined organics were dried over MgSO4
  4. customThe crude material (49 mg) was then purified by flash chromatography with a gradient of 5-100% EtOAc in hexane

出典と根拠

ORDレコード
ord-2e041e48bb7f4c2ba4b5bbbe97545663
出典データセット
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07960563B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート