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Hydrochloric Acid → HCID 178434312、化合物

HRID 392222
ノート
印刷プレビュー

反応式

HRID 392222 の反応式
S([N:8]1[C:16]2[C:11](=[CH:12][CH:13]=[C:14]([C:17]([O:19]C)=[O:18])[CH:15]=2)[C:10]([CH3:21])=[N:9]1)(C(F)(F)F)(=O)=O.C(=O)([O-])[O-].[K+].[K+].Cl>CO.O>[CH3:21][C:10]1[C:11]2[C:16](=[CH:15][C:14]([C:17]([OH:19])=[O:18])=[CH:13][CH:12]=2)[NH:8][N:9]=1
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 3

HCID 313Hydrochloric AcidHCID 11430Potassium CarbonateHCID 22663352Methyl 1-triflyl-3-methyl-indazole-6-carboxylate

生成物 1

HCID 178434312HCID 178434312、化合物収率 98.6%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 962Water溶媒
このページの内容参加物実験手順後処理出典と根拠反応ノート

実験手順

A solution of methyl 1-triflyl-3-methyl-indazole-6-carboxylate (0.668 g, Reference Example 46) in a mixture of methanol and water (3:1, 80 ml) was treated with potassium carbonate (1.15 g). The mixture was heated at reflux for 5 hours then cooled to room temperature then poured into 1N hydrochloric acid (50 ml). The mixture was extracted three times with ethyl acetate (50 ml). The combined extracts were dried over sodium sulphate then evaporated. The residue was washed with a mixture of hexane and ether to give the title compound (0.360 g).

後処理

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 5 hours
  3. extractionThe mixture was extracted three times with ethyl acetate (50 ml)
  4. dry with materialThe combined extracts were dried over sodium sulphate
  5. customthen evaporated
  6. washThe residue was washed with a mixture of hexane and ether

出典と根拠

ORDレコード
ord-2a2bc68542194ee38da35d014de3de4f
出典データセット
uspto-grants-2004_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06800645B1

反応ノート

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