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Methyl iodide → 7-Chloro-4-methyl-3-methylsulfanyl-4H-1,2,4-benzothiadiazine 1,1-dioxide

HRID 1066154
ノート
印刷プレビュー

反応式

HRID 1066154 の反応式
[Cl:1][C:2]1[CH:15]=[CH:14][C:5]2[NH:6][C:7]([S:12][CH3:13])=[N:8][S:9](=[O:11])(=[O:10])[C:4]=2[CH:3]=1.[C:16](=O)([O-])[O-].[K+].[K+].CI>C(#N)C.CO>[Cl:1][C:2]1[CH:15]=[CH:14][C:5]2[N:6]([CH3:16])[C:7]([S:12][CH3:13])=[N:8][S:9](=[O:11])(=[O:10])[C:4]=2[CH:3]=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 6328Methyl iodideHCID 11430Potassium CarbonateHCID 127001067-Chloro-3-(methylthio)-4H-benzo[e][1,2,4]thiadiazine 1,1-dioxide

生成物 1

HCID 211978047-Chloro-4-methyl-3-methylsulfanyl-4H-1,2,4-benzothiadiazine 1,1-dioxide

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 6342
Acetonitrile
溶媒

実験手順

A solution of 7-chloro-3-methylsulfanyl-4H-1,2,4-benzothiadiazine 1,1-dioxide (0.8 g) in acetonitrile (24 mL) and methanol (0.5 mL) was supplemented with potassium carbonate (0.96 g), then with methyl iodide (3 mL), and stirred at room temperature for 10 h. The solvent was removed by distillation under reduced pressure. The residue was suspended in water (40 mL) and the pH was adjusted to pH 2 with formic acid. The precipitate of the title compound was collected by filtration, washed with water and dried. The compound was used without further purification in the next step (yield: 0.53 g).

後処理

  1. customThe solvent was removed by distillation under reduced pressure
  2. filtrationThe precipitate of the title compound was collected by filtration
  3. washwashed with water
  4. customdried
  5. customThe compound was used without further purification in the next step (yield: 0.53 g)

出典と根拠

ORDレコード
ord-11bd17b8349c44cca3c109fcea3c9034
出典データセット
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06242443B1

反応ノート

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