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Methanol → HCID 53753295, 화합물

HRID 1264238
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HRID 1264238 반응식
[CH3:1][O:2][C:3]1[N:8]=[N:7][C:6]([C:9]2[CH:17]=[CH:16][C:12]([C:13]([OH:15])=[O:14])=[CH:11][CH:10]=2)=[CH:5][CH:4]=1.OS(O)(=O)=O.[CH3:23]O>>[CH3:23][O:14][C:13](=[O:15])[C:12]1[CH:16]=[CH:17][C:9]([C:6]2[N:7]=[N:8][C:3]([O:2][CH3:1])=[CH:4][CH:5]=2)=[CH:10][CH:11]=1
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참가 물질

4

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HCID 887MethanolHCID 1118Sulfuric AcidHCID 113566674-(6-methoxypyridazin-3-yl)benzoic Acid

생성물 1

HCID 53753295HCID 53753295, 화합물

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온도
50 °C

실험 절차

To a solution of 4-(6-methoxy-pyridazin-3-yl)-benzoic acid (5.02 g, 21.8 mmol) (reference example 11f) in methanol (75 mL) is added slowly conc. H2SO4 (3.75 mL). The resulting solution is heated to 50° C. and stirred for 1 hour. The solution is then concentrated to one third volume, cooled to 0°-5° C., adjusted to pH 6 with sat NaHCO3 soln and extracted into ethyl acetate. The organic layer is washed with brine, dried over MgSO4 and concentrated. The residue is purified by flash chromatography (eluting with 20% ethyl acetate in dichloromethane) to give 4.26 g of title compound as a white crystalline solid. 1H NMR (DMSO) δ 3.90 (s, 3H), 4.10 (s, 3H), 7.38 (d, J=9 Hz, 1H), 8.10 (d, J=9 Hz, 2H), 8.25 (m, 3H). MS (EI) m/z 244 (M+).

후처리

  1. concentrationThe solution is then concentrated to one third volume
  2. temperaturecooled to 0°-5° C.
  3. extractionextracted into ethyl acetate
  4. washThe organic layer is washed with brine
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated
  7. customThe residue is purified by flash chromatography (eluting with 20% ethyl acetate in dichloromethane)

출처 및 근거

ORD 기록
ord-82d5b5a6badf4685aab6a8efb9b96aa9
출처 데이터셋
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06541505B1

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