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Sodium Methoxide → 5-[3-(Methylsulfonylamino)propylthio]imidazo[1,2-a]pyridine

HRID 5472
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HRID 5472 반응식
[SH:1][C:2]1[N:7]2[CH:8]=[CH:9][N:10]=[C:6]2[CH:5]=[CH:4][CH:3]=1.C[O-].[Na+].[CH3:14][S:15]([NH:18][CH2:19][CH2:20][CH2:21]OS(C)(=O)=O)(=[O:17])=[O:16]>C(O)C>[CH3:14][S:15]([NH:18][CH2:19][CH2:20][CH2:21][S:1][C:2]1[N:7]2[CH:8]=[CH:9][N:10]=[C:6]2[CH:5]=[CH:4][CH:3]=1)(=[O:17])=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 10942334Sodium MethoxideHCID 233629523-Methylsulfonylamino-1-methylsulfonyloxypropaneHCID 178418687HCID 178418687, 화합물

생성물 1

HCID 233628535-[3-(Methylsulfonylamino)propylthio]imidazo[1,2-a]pyridine수율 47.5%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of 5-mercaptoimidazo[1,2-a]pyridine (1.50 g, 10 mmoles) and 4M sodium methylate (2.93 ml, 12 mmoles) in ethanol (50 ml) was added 3-methylsulfonylamino-1-methylsulfonyloxypropane (2.77 g, 12 mmoles) at room temperature and the mixture was heated under reflux for 16 hours. After cooling, the solvent was distilled off. The residue was dissolved in chloroform, washed with an aqueous saturated sodium bicarbonate solution and dried. After the solvent was distilled off, the residue was purified by column chromatography [eluent: ethyl acetate/ethanol (50:1)] to obtain 1.34 g of the desired product (47.5%, pale yellow crystals).

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 16 hours
  3. temperatureAfter cooling
  4. distillationthe solvent was distilled off
  5. dissolutionThe residue was dissolved in chloroform
  6. washwashed with an aqueous saturated sodium bicarbonate solution
  7. customdried
  8. distillationAfter the solvent was distilled off
  9. customthe residue was purified by column chromatography [eluent: ethyl acetate/ethanol (50:1)]

출처 및 근거

ORD 기록
ord-81bb6d68545c45f9ba9437d6d4437235
출처 데이터셋
uspto-grants-1993_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05244908

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