Methyl iodide → 6-Bromo-1-methyl-1H-indazole

HRID 2240515

反応式

HRID 2240515 の反応式
[Br:1][C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[N:7][NH:8]2)=[CH:4][CH:3]=1.[OH-].[K+].[CH3:13]I>CO.C(OCC)C>[Br:1][C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[N:7][N:8]2[CH3:13])=[CH:4][CH:3]=1

参加物

6

反応物 3

HCID 6328Methyl iodideHCID 14797Potassium HydroxideHCID 178424716-Bromo-1H-indazole

生成物 1

HCID 225586756-Bromo-1-methyl-1H-indazole

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 3283Diethyl Ether溶媒

実験手順

6-Bromoindazole (400 mg) was dissolved in methanol (10 mL). To this solution, potassium hydroxide (450 mg) was added followed by methyl iodide (0.50 mL) and the mixture was refluxed for 2.5 h. The reaction was cooled, diluted with diethyl ether, washed with water, brine, dried and concentrated. The product 6-bromo-1-methylindazole (160 mg) was separated from its isomer by Combiflash.

後処理

  1. temperaturethe mixture was refluxed for 2.5 h
  2. temperatureThe reaction was cooled
  3. washwashed with water, brine
  4. customdried
  5. concentrationconcentrated
  6. customThe product 6-bromo-1-methylindazole (160 mg) was separated from its isomer by Combiflash

出典と根拠

ORDレコード
ord-cee1e8295d9e4b999e0e3f6cac7ce064
出典データセット
uspto-grants-2010_05
特許番号
US07723349B2

関連ノート

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