Cyclohexylamine → HCID 178517975, compound
Reaction equation
S=[C:2]1[CH2:6][S:5][C:4](=[O:7])[NH:3]1.[CH:8]1([NH2:14])[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1>C(O)C>[CH:8]1([NH:14][C:2]2[CH2:6][S:5][C:4](=[O:7])[N:3]=2)[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 4-thioxo-1,3-thiazolidin-2-one (1.00 g) in ethanol (30 mL) was added cyclohexylamine (0.88 mL), and the mixture was heated under reflux overnight. The reaction mixture was concentrated under reduced pressure, the residue was purified by silica gel column chromatography (ethyl acetate/hexane), and the obtained powder was washed with ethyl acetate to give the title compound (599 mg).
Workup
- temperaturethe mixture was heated
- temperatureunder reflux overnight
- concentrationThe reaction mixture was concentrated under reduced pressure
- customthe residue was purified by silica gel column chromatography (ethyl acetate/hexane)
- washthe obtained powder was washed with ethyl acetate
Sources & evidence
- ORD record
- ord-62557213f626438cbb71da3c4d118dbf
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08772277B2
Reaction notes
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