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Water → 4-Chloro-1H-indazol-1-amine

HRID 842541
ノート
印刷プレビュー

反応式

HRID 842541 の反応式
[H-].[Na+].[Cl:3][C:4]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:5]=1[CH:6]=[N:7][NH:8]2.C1(C)C=C(C)C=C(C)C=1S(O[NH2:25])(=O)=O.O>O1CCCC1>[Cl:3][C:4]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:5]=1[CH:6]=[N:7][N:8]2[NH2:25]
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 24758Sodium hydrideHCID 3930374-Chloro-1H-indazoleHCID 11830845O-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamine2 回

生成物 1

HCID 226142584-Chloro-1H-indazol-1-amine収率 103.8%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran
溶媒
4 回

反応条件

温度
0 °C

実験手順

Sodium hydride (60 % wt suspension in mineral oil; 0.33 g, 8.3 mmol) is suspended in dry tetrahydrofuran (THF, 10 mL) and is cooled to 0° C. A mixture of 4-chloroindazole (1.05 g, 6.9 mmol) and THF (10 mL) is added to the slurry at 4° C. After the addition is completed, the mixture is stirred for 30 min. Then a mixture of O-mesitylenesulfonylhydroxylamine (1.25 g, 7 mmol) and THF (10 mL) is added slowly, at a temperature below 5° C. After the addition is completed, the reaction mixture is allowed to reach room temperature and is subsequently stirred for 3 h. Then the mixture is cooled again to 0° C., and a second aliquot of O-mesitylenesulfonylhydroxylamine (1.25 g, 7 mmol) in THF (10 mL) is added slowly. The mixture is allowed to reach ambient temperature and is subsequently stirred overnight. The reaction mixture is worked up by adding it to water, extracting into ethyl acetate, and drying over sodium sulfate. The crude product (1.2 g) is obtained after filtration of the drying agent and evaporation of the solvent. This material is used for the next reaction step without purification.

後処理

  1. additionis added to the slurry at 4° C
  2. additionAfter the addition
  3. additionis added slowly, at a temperature below 5° C
  4. additionAfter the addition
  5. customto reach room temperature
  6. stirringis subsequently stirred for 3 h
  7. temperatureThen the mixture is cooled again to 0° C.
  8. customto reach ambient temperature
  9. waitis subsequently stirred overnight
  10. extractionextracting into ethyl acetate
  11. dry with materialdrying over sodium sulfate

出典と根拠

ORDレコード
ord-728a1d1238f049ec94af763463600de1
出典データセット
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06376426B1

反応ノート

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