3-Methoxyaniline → HCID 178490983, compound
Reaction equation
[OH:1][C:2]1[C:7]([C:8]#[N:9])=[CH:6][N:5]=[C:4](SC)[N:3]=1.[CH3:12][O:13][C:14]1[CH:19]=[CH:18][CH:17]=[C:16]([NH2:20])[CH:15]=1>C(O)CCCC>[OH:1][C:2]1[C:7]([C:8]#[N:9])=[CH:6][N:5]=[C:4]([NH:20][C:16]2[CH:17]=[CH:18][CH:19]=[C:14]([O:13][CH3:12])[CH:15]=2)[N:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4-Hydroxy-2-(methylthio)pyrimidine-5-carbonitrile (3 mmol) and m-anisidine (3 mmol) in pentan-1-ol was refluxed for 40 h under nitrogen. The reaction mixture was concentrated in vacuo. The residue was washed with water and dried to afford 4-hydroxy-2-(3-methoxyphenylamino)pyrimidine-5-carbonitrile.
Workup
- concentrationThe reaction mixture was concentrated in vacuo
- washThe residue was washed with water
- customdried
Sources & evidence
- ORD record
- ord-40218cd3e9d248a39583346e7891bdb4
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08901143B2
Reaction notes
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