3-Pyridinemethanamine → HCID 57779898, compound
Reaction equation
CS[C:3]([N:8]1[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1)=[CH:4][N+:5]([O-:7])=[O:6].[N:14]1[CH:19]=[CH:18][CH:17]=[C:16]([CH2:20][NH2:21])[CH:15]=1>CCO>[N:8]1([C:3]([NH:21][CH2:20][C:16]2[CH:15]=[N:14][CH:19]=[CH:18][CH:17]=2)=[CH:4][N+:5]([O-:7])=[O:6])[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In 20 ml of EtOH was dissolved 0.8 g (0.004 mole) of 1-methylthio-1-piperidino-2-nitroethylene followed by addition of 0.4 g (0.004 mole) of 3-pyridylmethylamine. The mixture was refluxed for 2 hours. The ethanol was distilled off and the residue was purified by silica gel column chromatography to give 0.3 g of the title compound as a pale yellow powder.
Workup
- temperatureThe mixture was refluxed for 2 hours
- distillationThe ethanol was distilled off
- customthe residue was purified by silica gel column chromatography
Sources & evidence
- ORD record
- ord-1fb273fa10424701a1097c140283d966
- Source dataset
- uspto-grants-1999_08
- Patent number
- US05935981
Reaction notes
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