Dimethylamine → HCID 18952216, compound
Reaction equation
[O:1]1[CH2:6][CH2:5][N:4]([C:7]2[CH:12]=[CH:11][C:10]([C:13]([F:16])([F:15])[F:14])=[CH:9][C:8]=2[NH:17][C:18]([NH2:20])=S)[CH2:3][CH2:2]1.[OH-].[K+].[CH3:23][NH:24][CH3:25].O.O.O.C([O-])(=O)C.[Pb+2].C([O-])(=O)C>C(O)C>[CH3:23][N:24]([CH3:25])[C:18]([NH2:20])=[N:17][C:8]1[CH:9]=[C:10]([C:13]([F:16])([F:15])[F:14])[CH:11]=[CH:12][C:7]=1[N:4]1[CH2:5][CH2:6][O:1][CH2:2][CH2:3]1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 1-(2-morpholino-5-trifluoromethylphenyl)thiourea (6.1 g), potassium hydroxide (2.2 g), a 33% ethanolic solution of dimethylamine (5.6 ml), lead acetate trihydrate (7.5 g) and ethanol (40 ml) was heated at 90°-95° C. for 2 hours to yield 1,1-dimethyl-2-(2-morpholino-5-trifluoromethylphenyl)guanidine (m.p. 132°-135° C.) which was recrystallised from ethylacetate and converted into its fumarate salt (m.p. 228°-230° C.) which was recrystallised from a 1:2 mixture of methanol and ether.
Sources & evidence
- ORD record
- ord-c7de247ade5740f58e4e3f3de2b3aeb3
- Source dataset
- uspto-grants-1994_12
- Patent number
- US05373008
Reaction notes
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