Potassium Nitrate → HCID 19705062, compound
Reaction equation
[N+:1]([O-:4])([O-])=[O:2].[K+].[NH2:6][C:7]1[N:12]=[C:11]([NH2:13])[C:10]([C:14]2[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][C:15]=2[Cl:21])=[C:9]([CH3:22])[N:8]=1.C(=O)(O)[O-].[Na+]>S(=O)(=O)(O)O>[NH2:6][C:7]1[N:12]=[C:11]([NH2:13])[C:10]([C:14]2[CH:19]=[C:18]([N+:1]([O-:4])=[O:2])[C:17]([Cl:20])=[CH:16][C:15]=2[Cl:21])=[C:9]([CH3:22])[N:8]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Finely ground potassium nitrate (6.5 g 64 mmol) was added to a solution of 2,4-diamino-5-(2,4-dichlorophenyl)-6-methyl pyrimidine (17.23 g, 64 mmol) in concentrated sulphuric acid (150 ml). This mixture was stirred at room temperature for 90 minutes. The reaction mixture was then added to sodium bicarbonate and ice. The product was extracted with ethyl acetate. After the ethyl acetate was removed, a yellow solid was obtained (30.86 g). A portion of this crude product (7.0 g) was passed through a silica flash chromatography column and eluted with ethyl acetate to give the pure product (4.81 g).
Workup
- extractionThe product was extracted with ethyl acetate
- customAfter the ethyl acetate was removed
- customa yellow solid was obtained (30.86 g)
- washeluted with ethyl acetate
Sources & evidence
- ORD record
- ord-47d9f56e99084aeda417d35d94da66b8
- Source dataset
- uspto-grants-1997_01
- Patent number
- US05597828
Reaction notes
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