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Hydrochloric Acid → 2-Chloro-6-fluoro-5-methoxy-1,3-benzothiazole

HRID 2368096
ノート
印刷プレビュー

反応式

HRID 2368096 の反応式
N(OC(C)(C)C)=O.[F:8][C:9]1[C:18]([O:19][CH3:20])=[CH:17][C:12]2[N:13]=[C:14](N)[S:15][C:11]=2[CH:10]=1.[ClH:21]>C(#N)C.[Cl-].[Na+].O.[Cu](Cl)Cl>[Cl:21][C:14]1[S:15][C:11]2[CH:10]=[C:9]([F:8])[C:18]([O:19][CH3:20])=[CH:17][C:12]=2[N:13]=1
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

7

反応物 3

HCID 313Hydrochloric AcidHCID 10906Tert-Butyl nitriteHCID 57517493HCID 57517493、化合物

生成物 1

HCID 575174942-Chloro-6-fluoro-5-methoxy-1,3-benzothiazole

試薬・触媒・溶媒 3

HCID 24014Cupric Chloride触媒HCID 6342Acetonitrile溶媒2 回
HCID 57417360
Sodium chloride; water
溶媒

反応条件

温度
50 °C

実験手順

A suspension of copper(II) chloride (546 mg) and tert-butyl nitrite (0.600 mL) in acetonitrile (10 mL) was stirred at 50° C. for 20 min. To the reaction mixture was added a solution of 6-fluoro-5-methoxy-1,3-benzothiazol-2-amine (670 mg) in acetonitrile (10 mL), and the mixture was further stirred at 50° C. for 30 min. 1M Hydrochloric acid and saturated brine were added to the reaction mixture, and the insoluble material was filtered. The filtrate was extracted with ethyl acetate, the filtered insoluble material was dissolved in THF, and the solution was combined with the organic layer. The mixture was applied to silica gel column chromatography (ethyl acetate). The solvent was evaporated under reduced pressure and the obtained solid was washed with ethyl acetate/hexane to give the title compound (350 mg).

後処理

  1. stirringthe mixture was further stirred at 50° C. for 30 min
  2. filtrationthe insoluble material was filtered
  3. extractionThe filtrate was extracted with ethyl acetate
  4. dissolutionthe filtered insoluble material was dissolved in THF
  5. customThe solvent was evaporated under reduced pressure
  6. washthe obtained solid was washed with ethyl acetate/hexane

出典と根拠

ORDレコード
ord-c3eca9da52ee4295828810fab096eaa5
出典データセット
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08703758B2

反応ノート

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