HCID 13491770, compound → HCID 13491768, compound
Reaction equation
[CH3:1][C:2]1[C:7]([OH:8])=[C:6]([CH2:9][OH:10])[C:5]([CH2:11][S:12][C:13](=[O:20])[C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[CH:4][N:3]=1>C(Cl)(Cl)Cl>[CH3:1][C:2]1[C:7]([OH:8])=[C:6]([CH:9]=[O:10])[C:5]([CH2:11][S:12][C:13](=[O:20])[C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[CH:4][N:3]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of the 10 g. of the product from Step B in 300 ml. of hot chloroform was treated with 100 g. of maganese dioxide. After 1/2 hour of stirring, the mixture was filtered and the filtrate was evaporated to dryness to give 9.2 g. of 2-methyl-3-hydroxy-4-formyl-5-benzoylthiomethylpyrididne, m.p. 127°-130° C.
Workup
- filtrationthe mixture was filtered
- customthe filtrate was evaporated to dryness
- customto give 9.2 g
Sources & evidence
- ORD record
- ord-47cbf5e385de435f9f7323cccf8b3da5
- Source dataset
- uspto-grants-1977_12
- Patent number
- US04061759
Reaction notes
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