2-Mesitylenesulfonyl chloride → HCID 22731441, 화합물

HRID 2085551노트

반응식

HRID 2085551 반응식
[C:1]([C:6]1[CH:7]=[C:8]2[C:12](=[CH:13][CH:14]=1)[NH:11][CH:10]=[C:9]2[CH3:15])([O:3][CH2:4][CH3:5])=[O:2].[H-].[Na+].[CH3:18][C:19]1[CH:24]=[C:23]([CH3:25])[CH:22]=[C:21]([CH3:26])[C:20]=1[S:27](Cl)(=[O:29])=[O:28].[NH4+].[Cl-]>CN(C=O)C>[C:1]([C:6]1[CH:7]=[C:8]2[C:12](=[CH:13][CH:14]=1)[N:11]([S:27]([C:20]1[C:21]([CH3:26])=[CH:22][C:23]([CH3:25])=[CH:24][C:19]=1[CH3:18])(=[O:29])=[O:28])[CH:10]=[C:9]2[CH3:15])([O:3][CH2:4][CH3:5])=[O:2]

참가 물질

6

반응물 4

HCID 130462-Mesitylenesulfonyl chlorideHCID 24758Sodium hydrideHCID 25517Ammonium ChlorideHCID 12628587Ethyl 3-methyl-1H-indole-5-carboxylate

생성물 1

HCID 22731441HCID 22731441, 화합물수율 90%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a solution of 5-carboethoxy-3-methylindole (601 mg, 2.96 mmol) in DMF, sodium hydride (178 mg, 4.45 mmol) and 2,4,6-trimethylbenzenesulfonyl chloride (971 mg, 4.44 mmol) were added under cooling with ice, followed by stirring for 30 min. The reaction mixture was mixed with a saturated aqueous NH4Cl solution, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine. The organic layer was dried over magnesium sulfate and evaporated under reduced pressure to remove the solvent; the thus obtained residue was subjected to silica gel column chromatography (developing solvent: ethyl acetate:n-hexane=1:5) to give the titled compound (1.02 g, 90%).

후처리

  1. temperatureunder cooling with ice
  2. extractionextracted with ethyl acetate
  3. washThe organic layer was washed with water and saturated brine
  4. dry with materialThe organic layer was dried over magnesium sulfate
  5. customevaporated under reduced pressure
  6. customto remove the solvent

출처 및 근거

ORD 기록
ord-a5ca3c9e7f284be4990f017538c7b9e1
출처 데이터셋
uspto-grants-2004_04
특허 번호
US06720433B2

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