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Dimethyl Sulfate → 1-methyl-6-(3-pyridyl)-2-(1H)-quinolone

HRID 985993
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HRID 985993 반응식
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C:7]2[CH:8]=[C:9]3[C:14](=[CH:15][CH:16]=2)[NH:13][C:12](=[O:17])[CH:11]=[CH:10]3)[CH:2]=1.[H-].[Na+].S(OC)(O[CH3:24])(=O)=O>CN(C=O)C>[CH3:24][N:13]1[C:14]2[C:9](=[CH:8][C:7]([C:3]3[CH:2]=[N:1][CH:6]=[CH:5][CH:4]=3)=[CH:16][CH:15]=2)[CH:10]=[CH:11][C:12]1=[O:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6497Dimethyl SulfateHCID 24758Sodium hydrideHCID 99910956-(3-pyridyl)-2-(1H)-quinolone

생성물 1

HCID 137288561-methyl-6-(3-pyridyl)-2-(1H)-quinolone

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

실험 절차

A stirred solution of 6-(3-pyridyl)-2-[1H]-quinolone (0.05 g) in DMF (0.5 cm3) was treated at room temperature with sodium hydride (0.012 g of a 50% dispersion in oil) for 1 hour. A solution of dimethyl sulphate (0.016 g) in DMF (0.2 cm3) was added and the mixture was stirred for 1.5 hours. The mixture was concentrated in vacuo, water (5 cm3) was added and the mixture was extracted with ethyl acetate (3×10 cm3). The combined organic extracts were dried (MgSO4), concentrated in vacuo and the residue chromatographed on silica (Merck "MK 60.9385") eluting with chloroform to yield a solid which was triturated with ether to afford 1-methyl-6-(3-pyridyl)-2-(1H)-quinolone 0.25H2O, m.p. 116°-118°, (0.02 g).

후처리

  1. concentrationThe mixture was concentrated in vacuo, water (5 cm3)
  2. additionwas added
  3. extractionthe mixture was extracted with ethyl acetate (3×10 cm3)
  4. dry with materialThe combined organic extracts were dried (MgSO4)
  5. concentrationconcentrated in vacuo
  6. customthe residue chromatographed on silica (Merck "MK 60.9385")
  7. washeluting with chloroform
  8. customto yield a solid which
  9. customwas triturated with ether

출처 및 근거

ORD 기록
ord-d4eecf49b6734a2485ef314a7c5a0ccb
출처 데이터셋
uspto-grants-1987_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04710507

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