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Methyl iodide → 6-Bromo-1-methyl-1H-indazole-4-carbonitrile

HRID 520524
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HRID 520524 반응식
[H-].[Na+].[Br:3][C:4]1[CH:5]=[C:6]([C:13]#[N:14])[C:7]2[CH:8]=[N:9][NH:10][C:11]=2[CH:12]=1.I[CH3:16]>O1CCCC1>[Br:3][C:4]1[CH:5]=[C:6]([C:13]#[N:14])[C:7]2[CH:8]=[N:9][N:10]([CH3:16])[C:11]=2[CH:12]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 247289186-Bromo-1H-indazole-4-carbonitrile

생성물 1

HCID 666923166-Bromo-1-methyl-1H-indazole-4-carbonitrile수율 25%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
0 °C

실험 절차

Tetrahydrofuran (27 ml) was added to a flask containing sodium hydride (0.275 g, 6.89 mmol) and the mixture was stirred for 10 minutes at 0° C. 6-Bromo-1H-indazole-4-carbonitrile (1.39 g, 6.26 mmol) was added portionwise and the mixture was stirred for 10 mins until no further effervescence was seen. Iodomethane (0.431 ml, 6.89 mmol) was added and the mixture stirred at 0° C. for 1 h. The ice bath was removed and the flask was placed in a water bath at room temperature. The reaction remained stirring for 19 h and the mixture was then evaporated in vacuo. The residual solid purified by silica (100 g) cartridge using a gradient of ethyl acetate and cyclohexane to give the title compound as a white solid (370 mg).

후처리

  1. stirringthe mixture was stirred for 10 mins until no further effervescence
  2. stirringthe mixture stirred at 0° C. for 1 h
  3. customThe ice bath was removed
  4. customthe flask was placed in a water bath at room temperature
  5. stirringThe reaction remained stirring for 19 h
  6. customthe mixture was then evaporated in vacuo
  7. customThe residual solid purified by silica (100 g) cartridge

출처 및 근거

ORD 기록
ord-ac056bc358984bb08ceac37e96badeb7
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09326987B2

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