HCID 68577438, compound → 6-(Hydroxymethyl)-4-mercaptopyridin-3-ol
Reaction equation
C([O:4][CH2:5][C:6]1[CH:11]=[C:10]([S:12]C(C)(C)C)[C:9]([OH:17])=[CH:8][N:7]=1)(=O)C>Cl>[OH:4][CH2:5][C:6]1[N:7]=[CH:8][C:9]([OH:17])=[C:10]([SH:12])[CH:11]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 80 °C
Procedure
{4-[(1,1-dimethylethyl)thio]-5-hydroxy-2-pyridinyl}methyl acetate (2.5 g, 9.8 mmol) was dissolved in concentrated HCl and the mixture was heated at 80° C. for 18 hours. The solvent was evaporated under vacuum and the residue was triturated with diethyl ether to afford the product as a solid (1.35 g, 88%); MS (+ve ion electrospray) m/z 158 (MH+).
Workup
- customThe solvent was evaporated under vacuum
- customthe residue was triturated with diethyl ether
Sources & evidence
- ORD record
- ord-f23a8eee1ff24bcd9621e1c8230efd84
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07691850B2
Reaction notes
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