Sodium hydride → HCID 178424719, compound
Reaction equation
[CH3:1][C:2]1[C:3]([N+:15]([O-:17])=[O:16])=[C:4]([CH:12]=[CH:13][CH:14]=1)[C:5]([NH:7][O:8][CH2:9][CH2:10]Cl)=[NH:6].[H-].[Na+]>CN1CCCC1=O>[CH3:1][C:2]1[C:3]([N+:15]([O-:17])=[O:16])=[C:4]([C:5]2[NH:6][CH2:10][CH2:9][O:8][N:7]=2)[CH:12]=[CH:13][CH:14]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 100 °C
Procedure
1.4 g (5.4 mmol) of 3-methyl-N-(2-chloroethoxy)-2-nitrobenzamidine are initially charged in 45 ml of 1-methyl-2-pyrrolidone, and 0.18 g (6 mmol) of sodium hydride (80% pure) is added slowly. The mixture is stirred at 100° C. for 12 h, cooled, poured onto water and extracted with ethyl acetate. After drying over sodium sulphate, the solvent is distilled off under reduced pressure.
Workup
- temperaturecooled
- additionpoured onto water
- extractionextracted with ethyl acetate
- dry with materialAfter drying over sodium sulphate
- distillationthe solvent is distilled off under reduced pressure
Sources & evidence
- ORD record
- ord-3d409fb4d36f46b1b1a5268f4debe14b
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08062995B2
Reaction notes
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