HCID 13922926, compound → HCID 178448724, compound
Reaction equation
[C:1]([C:3]1[C:8]([O:9][CH3:10])=[C:7]([O:11][CH3:12])[CH:6]=[CH:5][C:4]=1[NH:13][C:14]([NH:16][CH2:17][CH2:18][CH2:19][CH3:20])=[O:15])#[N:2]>C[O-].[Na+]>[CH2:17]([N:16]1[C:1](=[NH:2])[C:3]2[C:4](=[CH:5][CH:6]=[C:7]([O:11][CH3:12])[C:8]=2[O:9][CH3:10])[NH:13][C:14]1=[O:15])[CH2:18][CH2:19][CH3:20]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 1-(2-cyano-3,4-dimethoxyphenyl)-3-butyl urea (5.2 g, 18.8 mmol) in 50 ml of 0.5N methanolic sodium methoxide was heated at reflux under nitrogen for 18 hours. The reaction solution was cooled and a precipitate which formed was collected, washed with cold methanol and dried giving 3.61 g (68.4%) of analytical product, mp 165°-168°.
Workup
- temperaturewas heated
- temperatureat reflux under nitrogen for 18 hours
- temperatureThe reaction solution was cooled
- customa precipitate which formed
- customwas collected
- washwashed with cold methanol
- customdried
Sources & evidence
- ORD record
- ord-b78292f112d7482e988d3cfb3f8b2c6f
- Source dataset
- uspto-grants-1987_05
- Patent number
- US04668787
Reaction notes
Loading…