HCID 19912998, compound → HCID 19912992, compound
Reaction equation
[OH:1][CH2:2][C:3]1[CH:8]=[C:7]([NH:9][C:10](=[O:12])[CH3:11])[CH:6]=[CH:5][N:4]=1>ClCCl>[C:10]([NH:9][C:7]1[CH:6]=[CH:5][N:4]=[C:3]([CH:2]=[O:1])[CH:8]=1)(=[O:12])[CH3:11]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
2 g of the thus obtained 2-hydroxymethyl-4-acetylaminopyridine were suspended in 400 ml of dichloromethane, mixed with 6 g of MnO3 refluxed for 26 hours. The MnO2 was then filtered hot and the dichloromethane solution rotated n to dryness. 1.5 g of 4-acetylaminopyridine-2-aldehyde were obtained.
Workup
- temperaturerefluxed for 26 hours
- filtrationThe MnO2 was then filtered hot
Sources & evidence
- ORD record
- ord-41ff300a51264466bd016fb53f1e3ee8
- Source dataset
- uspto-grants-1992_01
- Patent number
- US05084458
Reaction notes
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