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Ethanol → Bromo-4-oxo-3,4-dihydro-phthalazine-6-carboxylic acid ethyl ester

HRID 1783721
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HRID 1783721 반응식
S(=O)(=O)(O)O.[Br:6][C:7]1[C:16]2[C:11](=[CH:12][C:13]([C:17]([OH:19])=[O:18])=[CH:14][CH:15]=2)[C:10](=[O:20])[NH:9][N:8]=1.[CH3:21][CH2:22]O>>[CH2:21]([O:18][C:17]([C:13]1[CH:12]=[C:11]2[C:16](=[CH:15][CH:14]=1)[C:7]([Br:6])=[N:8][NH:9][C:10]2=[O:20])=[O:19])[CH3:22]
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참가 물질

4

반응물 3

HCID 702EthanolHCID 1118Sulfuric AcidHCID 211065111-Bromo-4-oxo-3,4-dihydro-phthalazine-6-carboxylic acid

생성물 1

HCID 57856207Bromo-4-oxo-3,4-dihydro-phthalazine-6-carboxylic acid ethyl ester수율 31%

실험 절차

Concentrated sulfuric acid (40 ml) was added to a stirred solution of 1-bromo-4-oxo-3,4-dihydro-phthalazine-6-carboxylic acid (85 g, 0.32 mol) in EtOH (500 ml) and the mixture was heated to reflux for 48 hours. After this time, the reaction mixture was cooled and the resulting precipitate was filtered. The precipitate was partitioned between EtOAc (1 L) and saturated NaHCO3 (500 ml), the organic layer was separated and washed with water (500 ml) before being dried (MgSO4), filtered and concentrated under vacuum to give the title compound (30 g, 31% yield) as a white solid. Tr=1.23 min, m/z (ES+) (M+H)+ 297 & 299

후처리

  1. temperaturethe mixture was heated
  2. temperatureto reflux for 48 hours
  3. temperatureAfter this time, the reaction mixture was cooled
  4. filtrationthe resulting precipitate was filtered
  5. customThe precipitate was partitioned between EtOAc (1 L) and saturated NaHCO3 (500 ml)
  6. customthe organic layer was separated
  7. washwashed with water (500 ml)
  8. dry with materialbefore being dried (MgSO4)
  9. filtrationfiltered
  10. concentrationconcentrated under vacuum

출처 및 근거

ORD 기록
ord-51191748fff74f2bbc598516fa53700f
출처 데이터셋
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07501410B2

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