4-Methoxyphenylhydrazine hydrochloride → HCID 10778313, compound
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=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
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 vacuo. 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
- temperaturewas refluxed for 5 hours
- temperatureThe reaction mixture was cooled
- filtrationfiltrated through a pad of Celite
- customto remove any solids in the mixture
- customThe solvent was removed in vacuo
- customThe remaining residue was partitioned between EtOAc and saturated NaHCO3
- extractionThe aqueous phase was extracted two times with EtOAc
- extractionThe organic layer of each extraction
- washwas washed with water, brine
- dry with materialdried over anhydrous Na2SO4
- filtrationfiltered
- concentrationconcentrated
- customto yield a brown oil
- customThe crude material (the oil) was then purified by column chromatography (silica gel, hexanes: EtOAc1:1 as eluent)
Sources & evidence
- ORD record
- ord-63e295d50fed4ea8a340cd14559cf055
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07696239B2
Reaction notes
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