3,5-Dimethylpyrazole → HCID 18507538, compound

HRID 1356169Notes

Reaction equation

HRID 1356169 reaction equation
[NH2:1][C:2]1[N:7]=[C:6](Br)[C:5]([C:9]#[N:10])=[C:4]([S:11][CH3:12])[N:3]=1.[CH3:13][C:14]1[CH:18]=[C:17]([CH3:19])[NH:16][N:15]=1.C(=O)([O-])[O-].[Cs+].[Cs+]>CN1C(=O)CCC1>[NH2:1][C:2]1[N:7]=[C:6]([N:15]2[C:14]([CH3:13])=[CH:18][C:17]([CH3:19])=[N:16]2)[C:5]([C:9]#[N:10])=[C:4]([S:11][CH3:12])[N:3]=1

Participants

5

Reactant 3

HCID 62103,5-DimethylpyrazoleHCID 10796Cesium carbonateHCID 187532302-Amino-4-bromo-6-methylsulfanyl-pyrimidine-5-carbonitrile

Product 1

HCID 18507538HCID 18507538, compound

Reagents, catalysts & solvents 1

HCID 13387N-methyl-2-pyrrolidoneSolvent

Procedure

From 2-amino-4-bromo-6-methylsulfanyl-pyrimidine-5-carbonitrile, 3,5-dimethylpyrazole and cesium carbonate in NMP. EI-MS m/e (%): 259 ([M—H]−, 100).

Sources & evidence

ORD record
ord-312642427917491681cacedd8578c77a
Source dataset
uspto-grants-2003_07
Patent number
US06586441B2

Reaction notes

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