Water → 5-Chloro-6-(3-fluorophenyl)-2-methyl-[1,2,4]triazolo[1,5-a]pyrimidine
Reaction equation
[Cl:1][C:2]1[C:7]([C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([F:14])[CH:9]=2)=[C:6](Cl)[N:5]2[N:16]=[C:17]([CH3:19])[N:18]=[C:4]2[N:3]=1.[NH4+].[Cl-].O.C1COCC1>C(O)C.[Zn]>[Cl:1][C:2]1[C:7]([C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([F:14])[CH:9]=2)=[CH:6][N:5]2[N:16]=[C:17]([CH3:19])[N:18]=[C:4]2[N:3]=1Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
10.4 g (35 mmol) 5,7-Dichloro-6-(3-fluorophenyl)-2-methyl-[1,2,4]triazolo[1,5-a]pyrimidine are given in 898 mL ethanol. 8.8 g (164.5 mmol) NH4Cl, 630 mL water, 340 mL THF and 14.6 g (224 mmol) zinc powder are added. The mixture is stirred at room temperature for 3.5 hours. The reaction mixture is filtered and the organic solvents are removed. The residue is diluted with water and extracted three times with ethyl acetate. The combined organic layers are washed with brine and dried over Na2SO4. After evaporation of the solvent the residue is purified by chromatography giving 0.73 g (7.9%) of the desired product. Due to this low yield the zinc- and the Na2SO4 filter cakes are extracted with methanol delivering 2.3 g starting material.
Workup
- filtrationThe reaction mixture is filtered
- customthe organic solvents are removed
- additionThe residue is diluted with water
- extractionextracted three times with ethyl acetate
- washThe combined organic layers are washed with brine
- dry with materialdried over Na2SO4
- customAfter evaporation of the solvent the residue
- customis purified by chromatography
Sources & evidence
- ORD record
- ord-3dd1eb510e8b4931a2b35eaa320c629e
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08957064B2
Reaction notes
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