4-Methoxyphenylhydrazine hydrochloride → HCID 10778313, compound

HRID 1391692Notes

Reaction equation

HRID 1391692 reaction equation
[S:1]1[C:6]2=[N:7][CH:8]=[CH:9][CH:10]=[C:5]2[C:4](=O)[CH2:3][CH2:2]1.Cl.[CH3:13][O:14][C:15]1[CH:20]=[CH:19][C:18]([NH:21]N)=[CH:17][CH:16]=1>CCO>[CH3:13][O:14][C:15]1[CH:16]=[C:17]2[C:18](=[CH:19][CH:20]=1)[NH:21][C:4]1[C:5]3[CH:10]=[CH:9][CH:8]=[N:7][C:6]=3[S:1][CH2:2][C:3]2=1

Participants

4

Procedure

A mixture of 2,3-dihydro-thiopyrano[2,3-b]pyridin-4-one (2.24 g, 13.6 mmoL) and 4-methoxy-phenylhydrazine HCl salt (2.60 g, 14.9 mmoL) in EtOH (10 mL) was refluxed for 5 hours. The reaction mixture was cooled and filtrated through a pad of Celite to remove any solids in the mixture. The solvent was removed in vacua. The remaining residue was partitioned between EtOAc and saturated NaHCO3. The aqueous phase was extracted two times with EtOAc. The organic layer of each extraction was washed with water, brine, dried over anhydrous Na2SO4, filtered and concentrated to yield a brown oil. The crude material (the oil) was then purified by column chromatography (silica gel, hexanes:EtOAc1:1 as eluent) to yield the title compound as a pale solid.

Workup

  1. temperaturewas refluxed for 5 hours
  2. temperatureThe reaction mixture was cooled
  3. filtrationfiltrated through a pad of Celite
  4. customto remove any solids in the mixture
  5. customThe solvent was removed in vacua
  6. customThe remaining residue was partitioned between EtOAc and saturated NaHCO3
  7. extractionThe aqueous phase was extracted two times with EtOAc
  8. extractionThe organic layer of each extraction
  9. washwas washed with water, brine
  10. dry with materialdried over anhydrous Na2SO4
  11. filtrationfiltered
  12. concentrationconcentrated
  13. customto yield a brown oil
  14. customThe crude material (the oil) was then purified by column chromatography (silica gel, hexanes:EtOAc1:1 as eluent)

Sources & evidence

ORD record
ord-760b6874d9f84af599a51e5c747cff38
Source dataset
uspto-grants-2008_03
Patent number
US07338973B2

Reaction notes

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