Cyanamide → HCID 10241976, compound
Reaction equation
[CH3:1][C:2]1[CH:3]=[C:4]([C:8](=[NH:13])[O:9][CH2:10][CH2:11][CH3:12])[CH:5]=[N:6][CH:7]=1.[N:14]#[C:15]N>>[C:15]([N:13]=[C:8]([C:4]1[CH:5]=[N:6][CH:7]=[C:2]([CH3:1])[CH:3]=1)[O:9][CH2:10][CH2:11][CH3:12])#[N:14]Participants
3
Procedure
To propyl 5-methyl-3-pyridinecarboximidate was then added an aqueous solution (100 ml) of cyanamide (1.42 g, 33.8 mmol), Na2HPO4 (2.40 g, 16.9 mmol) and NaH2PO4 ·2H2O (10.56 g, 67.7 mmol). The mixture was stirred at room temperature for 5 hours and extracted with chloroform (100 ml×3). The chloroform layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give a crude product of propyl N-cyano-5-methyl-3-pyridinecarboximidate (2.54 g). IR (neat) cm-1 : 2200, 1610, 1320, 730.
Workup
- extractionextracted with chloroform (100 ml×3)
- dry with materialThe chloroform layer was dried over anhydrous sodium sulfate
- concentrationconcentrated under reduced pressure
Sources & evidence
- ORD record
- ord-3ee806ad00ad4694bdaefcc20e72927a
- Source dataset
- uspto-grants-1996_04
- Patent number
- US05508293
Reaction notes
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