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

HRID 2368096
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HRID 2368096 반응식
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
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참가 물질

7

반응물 3

HCID 313Hydrochloric AcidHCID 10906Tert-Butyl nitriteHCID 57517493HCID 57517493, 화합물

생성물 1

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

시약·촉매·용매 3

HCID 24014Cupric Chloride촉매HCID 6342Acetonitrile용매2회
HCID 57417360
Sodium chloride; water
용매

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온도
50 °C

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-c3eca9da52ee4295828810fab096eaa5
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08703758B2

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