Dimethylformamide dimethyl acetal → 1-(2',6'-Dimethylphenyl)-4-amino-1,2-dihydro-1,3,5-triazin-2-one
Reaction equation
Cl.[CH3:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([CH3:9])[C:4]=1[NH:10][C:11]([NH:13][C:14]([NH2:16])=O)=N.C[O:18][CH:19](OC)[N:20](C)C>CC#N>[CH3:9][C:5]1[CH:6]=[CH:7][CH:8]=[C:3]([CH3:2])[C:4]=1[N:10]1[CH:11]=[N:13][C:14]([NH2:16])=[N:20][C:19]1=[O:18]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a magnetically stirred suspension of 9.7 g. (40 mmol) of 1-(2',6'-dimethylphenyl)amidinourea hydrochloride in 50 ml. of CH3CN at room temperature is added 5.7 g. (48 mmol) of N,N-dimethylformamide dimethylacetal. The reaction mixture is stirred for 10 minutes after which all of the solid material goes into solution. The solution is stirred for 5 minutes after which a seed crystal is added. A white solid precipitates. The reaction mixture is stirred for an additional 1.5 hours, after which the solid precipitate is filtered to yield 1-(2',6'-dimethylphenyl)-4-amino-1,2-dihydro-1,3,5-triazin-2-one, melting point 248.5°-249.5° C. When recrystallized from absolute EtOH the product is obtained as a white solid with melting point 258.6°-259° C.
Workup
- additionTo a magnetically stirred suspension of 9.7 g
- stirringThe solution is stirred for 5 minutes after which a seed crystal
- additionis added
- customA white solid precipitates
- stirringThe reaction mixture is stirred for an additional 1.5 hours
- filtrationafter which the solid precipitate is filtered
Sources & evidence
- ORD record
- ord-921067d9c8ae4baf87971a69be572d3f
- Source dataset
- uspto-grants-1982_07
- Patent number
- US04338441
Reaction notes
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