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6-(methylsulfanyl)-1H-indole-2-carboxylic acid → 6-(Methylsulfanyl)-1H-indole

HRID 442752
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인쇄 미리보기

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HRID 442752 반응식
[CH3:1][S:2][C:3]1[CH:11]=[C:10]2[C:6]([CH:7]=[C:8](C(O)=O)[NH:9]2)=[CH:5][CH:4]=1>N1C2C(=CC=CC=2)C=CC=1>[CH3:1][S:2][C:3]1[CH:11]=[C:10]2[C:6]([CH:7]=[CH:8][NH:9]2)=[CH:5][CH:4]=1
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참가 물질

3

반응물 1

HCID 39071736-(methylsulfanyl)-1H-indole-2-carboxylic acid

생성물 1

HCID 198489176-(Methylsulfanyl)-1H-indole수율 90.6%

시약·촉매·용매 1

HCID 7047Quinoline용매

반응 조건

온도
215 °C

실험 절차

A mixture of 6-methylsulfanyl-1H-indole-2-carboxylic acid (9.6 g, 46 mmol), Cu powder (2.1 g, 33 mmol) and quinoline (100 ml) was heated at 215° C. for 3 hours. The mixture was cooled to room temperature, filtered through celite, and the filtrate diluted with H2O (500 mL). The cooled mixture was acidified with concentrated HCl (pH=1), and extracted with EtOAc. The organic fraction was washed with saturated NaCl solution, dried over MgSO4, filtered and evaporated to give of 6-Methylsulfanyl-1H-indole (6.8 g, 90%) after purification by flash column chromatography.

후처리

  1. temperatureThe mixture was cooled to room temperature
  2. filtrationfiltered through celite
  3. additionthe filtrate diluted with H2O (500 mL)
  4. extractionextracted with EtOAc
  5. washThe organic fraction was washed with saturated NaCl solution
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. customevaporated

출처 및 근거

ORD 기록
ord-1e46f9022ba945e697bdd1f5b670b94d
출처 데이터셋
uspto-grants-1999_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05891901

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