Methylamine → HCID 14369789, compound
Reaction equation
[CH3:1][NH2:2].[CH3:3][C:4]1[N:5]=[C:6]([C:15]([O:17]C)=O)[S:7][C:8]=1[C:9]1[CH:14]=[CH:13][N:12]=[CH:11][CH:10]=1>C(O)C>[CH3:1][NH:2][C:15]([C:6]1[S:7][C:8]([C:9]2[CH:10]=[CH:11][N:12]=[CH:13][CH:14]=2)=[C:4]([CH3:3])[N:5]=1)=[O:17]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Methyl amine (0.5 ml) was added to a stirred solution of methyl 4-methyl-5-(4-pyridinyl)-thiazole-2-carboxylate (250 mg) in absolute ethanol (10 ml) at room temperature, and the mixture was stirred at room temperature for overnight. The mixture was evaporated to dryness and the residue was recrystallized from iso-propanol to give N,4-dimethyl-5-(4-pyridinyl)-thiazole-2-carboxamide (200 mg, yield 80.0%) as pale yellow needles.
Workup
- customThe mixture was evaporated to dryness
- customthe residue was recrystallized from iso-propanol
Sources & evidence
- ORD record
- ord-bc92dde5e4354d728c4fe8fcb5f3982c
- Source dataset
- uspto-grants-1989_02
- Patent number
- US04804668
Reaction notes
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