Trifluoroacetic acid → HCID 178506407、化合物

HRID 246721

反応式

HRID 246721 の反応式
[F:1][CH:2]([F:21])[O:3][C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[N:9](C(OC(C)(C)C)=O)[N:8]=[C:7]2[I:20].FC(F)(F)C(O)=O>ClCCl>[F:21][CH:2]([F:1])[O:3][C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[NH:9][N:8]=[C:7]2[I:20]

参加物

4

反応物 2

HCID 6422Trifluoroacetic acidHCID 71279601tert-butyl 5-(difluoromethoxy)-3-iodo-1H-indazole-1-carboxylate

生成物 1

HCID 178506407HCID 178506407、化合物収率 97%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a stirred solution of tert-butyl 5-(difluoromethoxy)-3-iodo-1H-indazole-1-carboxylate (410 mg, 1 mmol) in dichloromethane (10 mL) was added drop-wise trifluoroacetic acid (5 mL) at room temperature and the reaction mixture was stirred for 1 hour. The mixture was washed with NaHCO3 aqueous, and then organic was dried over Na2SO4. After filtration and concentration, 5-(difluoromethoxy)-3-iodo-1H-indazole (300 mg, 97%) was obtained as a white solid, used in the next step without further purification. MS: (M+H)+=311.

後処理

  1. washThe mixture was washed with NaHCO3 aqueous
  2. dry with materialorganic was dried over Na2SO4
  3. filtrationAfter filtration and concentration

出典と根拠

ORDレコード
ord-8ce6ca9075bf4c15bd54f5e18f9a43b0
出典データセット
uspto-grants-2014_02
特許番号
US08658646B2

関連ノート

読み込み中…