Piperidine → HCID 178429185, compound
Reaction equation
[NH2:1][C:2]1[N:6]=[C:5]([SH:7])[NH:4][N:3]=1.[C:8](OCC)(=[O:13])[CH2:9][C:10]([CH3:12])=O.N1CCCCC1>C(O)C>[OH:13][C:8]1[N:3]2[N:4]=[C:5]([SH:7])[N:6]=[C:2]2[N:1]=[C:10]([CH3:12])[CH:9]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 3-amino-5-mercapto-s-triazole (10 g), ethyl acetoacetate (34 g), piperidine (10 ml) and ethanol (300 ml) was refluxed for four hours. After removing the solvent by distillation under reduced pressure, 150 ml water was added, the mixture was neutralized to pH 7.0 with hydrochloric acid and cooled, giving 5.9 g of the objective compound.
Workup
- temperaturewas refluxed for four hours
- customAfter removing the solvent
- distillationby distillation under reduced pressure, 150 ml water
- additionwas added
- temperaturecooled
Sources & evidence
- ORD record
- ord-da9e5a02aec943218c6689899b198de5
- Source dataset
- uspto-grants-1991_11
- Patent number
- US05064953
Reaction notes
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