Reaction equation
[CH3:1][N:2]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)[C:3]([NH2:5])=[S:4].CO[CH:14](OC)[CH2:15]Cl>C1(C)C=CC=CC=1>[CH3:1][N:2]([C:3]1[S:4][CH:14]=[CH:15][N:5]=1)[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 10 g (60 mmol) of N-methyl-N-phenylthiourea in 100 mL of toluene was treated with 7.2 mL (63 mmol) of chloroacetaldehyde dimethylacetal and heated at reflux for 12 h. The solvent was removed in vacuo and the residue purified by flash chromatography eluting with a linear gradient of 30% EtOAc in hexane to 80% EtOAc in hexane to deliver the title compound. MS (M+H)+ 191.
Workup
- temperatureheated
- temperatureat reflux for 12 h
- customThe solvent was removed in vacuo
- customthe residue purified by flash chromatography
- washeluting with a linear gradient of 30% EtOAc in hexane to 80% EtOAc in hexane
Sources & evidence
- ORD record
- ord-02e610bd787749ae9e8cb99fa034b663
- Source dataset
- uspto-grants-2010_08
- Patent number
- US07786132B2
Linked notes
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