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Water → 5-Bromo-1-(3-fluoro-4-hydroxyphenyl)-1H-indazol-4-ol

HRID 2423104
ノート
印刷プレビュー

反応式

HRID 2423104 の反応式
[Br:1][C:2]1[C:3]([O:26]C)=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([C:11]1[CH:16]=[CH:15][C:14]([O:17]CC3C=CC=CC=3)=[C:13]([F:25])[CH:12]=1)[N:6]=[CH:5]2.B(Br)(Br)Br.O.C(OCC)(=O)C>ClCCl>[Br:1][C:2]1[CH:10]=[CH:9][C:8]2[N:7]([C:11]3[CH:16]=[CH:15][C:14]([OH:17])=[C:13]([F:25])[CH:12]=3)[N:6]=[CH:5][C:4]=2[C:3]=1[OH:26]
参加物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 8857Ethyl AcetateHCID 25134Boron tribromideHCID 592729765-Bromo-1-{3-fluoro-4-[(phenylmethyl)oxy]phenyl}-4-(methyloxy)-1H-indazole

生成物 1

HCID 1359103655-Bromo-1-(3-fluoro-4-hydroxyphenyl)-1H-indazol-4-ol収率 74.5%

試薬・触媒・溶媒 1

HCID 6344
Dichloromethane
溶媒

実験手順

A solution of 5-bromo-1-{3-fluoro-4-[(phenylmethyl)oxy]phenyl}-4-(methyloxy)-1H-indazole (D20) (71 mg) in dry dichloromethane (2 mL) was cooled to −78° C. under argon and treated dropwise with boron tribromide solution (0.75 mL of 1M solution in dichloromethane, 0.75 mmol). The mixture was allowed to reach room temperature and was stirred overnight. Water and ethyl acetate were added and the pH of the aqueous layer was adjusted to 7 and the product was extracted into ethyl acetate. The extracts were dried (Na2SO4), concentrated and chromatographed (silica gel, 0-100% ethyl acetate in hexane) to give the title compound (E11) as a beige solid (40 mg)

後処理

  1. customto reach room temperature
  2. extractionthe product was extracted into ethyl acetate
  3. dry with materialThe extracts were dried (Na2SO4)
  4. concentrationconcentrated
  5. customchromatographed (silica gel, 0-100% ethyl acetate in hexane)

出典と根拠

ORDレコード
ord-4c8adedf33174b289b4e8c5b249e9ffd
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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