Water → HCID 136167197, compound

HRID 646457Notes

Reaction equation

HRID 646457 reaction equation
Cl.[NH2:2]O.[OH:4][C:5]1[CH:14]=[C:13]2[C:8]([C:9](=[O:24])[C:10]([C:16]3[CH:21]=[CH:20][C:19]([O:22][CH3:23])=[CH:18][CH:17]=3)=[C:11]([CH3:15])[O:12]2)=[CH:7][C:6]=1[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1.O>N1C=CC=CC=1>[CH3:23][O:22][C:19]1[CH:20]=[CH:21][C:16]([C:10]2[C:11]([CH3:15])=[N:2][O:24][C:9]=2[C:8]2[CH:7]=[C:6]([C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)[C:5]([OH:4])=[CH:14][C:13]=2[OH:12])=[CH:17][CH:18]=1

Participants

5

Procedure

Hydroxylamine hydrochloride (75 mg, 1.08 mmol) was added to a suspension of 7-hydroxy-3-(4-methoxy-phenyl)-2-methyl-6-phenyl-chromen-4-one (105 mg, 0.29 mmol) in pyridine (2 ml) and the mixture heated under reflux for ˜6 hrs., to give a pale yellow solution. The solution was allowed to cool and water (20 ml) added. The mixture was extracted with diethyl ether (2×10 ml). The combined extracts were washed with water (2×20 ml) and saturated aqueous sodium chloride solution (10 ml). The solution was dried over anhydrous magnesium sulphate and concentrated. The crude products were purified by column chromatography, silica, eluting with ethyl acetate/hexane (1:1), to give the title compound as an off-white powder (80 mg)

Workup

  1. temperaturethe mixture heated
  2. temperatureunder reflux for ˜6 hrs
  3. custom, to give a pale yellow solution
  4. temperatureto cool
  5. extractionThe mixture was extracted with diethyl ether (2×10 ml)
  6. washThe combined extracts were washed with water (2×20 ml) and saturated aqueous sodium chloride solution (10 ml)
  7. dry with materialThe solution was dried over anhydrous magnesium sulphate
  8. concentrationconcentrated
  9. customThe crude products were purified by column chromatography, silica
  10. washeluting with ethyl acetate/hexane (1:1)

Sources & evidence

ORD record
ord-63e2569b1674409e8f5a62400887d9e8
Source dataset
uspto-grants-2010_04
Patent number
US07705027B2

Reaction notes

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