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Hydrochloric Acid → HCID 178504658, 화합물

HRID 1749932
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HRID 1749932 반응식
[CH3:1][S:2]([C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][CH:13]=1)[NH:10]C=C2)(=[O:4])=[O:3].O.[N:15]([O-])=O.[Na+].Cl.[O:20]1[CH2:25][CH2:24]OCC1>>[CH3:1][S:2]([C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][CH:13]=1)[NH:10][N:15]=[C:24]2[CH:25]=[O:20])(=[O:4])=[O:3]
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참가 물질

6

반응물 5

HCID 313Hydrochloric AcidHCID 962WaterHCID 312751,4-DioxaneHCID 149732305-(Methylsulfonyl)-1H-indoleHCID 23668193Sodium Nitrite

생성물 1

HCID 178504658HCID 178504658, 화합물수율 25%

실험 절차

A solution of 5-(methylsulfonyl)-1H-indole (0.150 g, 0.768 mmol) in 1,4-dioxane (8 mL) was added with water (96 mL), and the mixture was stirred at room temperature. The reaction mixture was added with sodium nitrite (0.530 g, 7.68 mmol), and the mixture was cooled to 0° C. The reaction mixture was added dropwise with 3 N hydrochloric acid (1.54 mL, 4.62 mmol) at 0° C., and then the mixture was stirred at room temperature for 3 hours. The reaction mixture was extracted three times with ethyl acetate, and then the organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The organic layer was concentrated, and the resulting residue was purified by silica gel column chromatography (chloroform/methanol) to obtain 5-(methylsulfonyl)-1H-indazole-3-carboxaldehyde (0.0433 g, 25%).

후처리

  1. temperaturethe mixture was cooled to 0° C
  2. stirringthe mixture was stirred at room temperature for 3 hours
  3. extractionThe reaction mixture was extracted three times with ethyl acetate
  4. washthe organic layer was washed with saturated brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. concentrationThe organic layer was concentrated
  7. customthe resulting residue was purified by silica gel column chromatography (chloroform/methanol)

출처 및 근거

ORD 기록
ord-5cdabed5cab64e06b6f1b3875c5a89ca
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09156827B2

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