2-Amino-5-bromopyrimidine → HCID 86654457, compound

HRID 552633Notes

Reaction equation

HRID 552633 reaction equation
[NH2:1][C:2]1[N:7]=[CH:6][C:5]([Br:8])=[CH:4][N:3]=1.[Cl:9][C:10]1[CH:11]=[C:12]([C:17]2([C:32]([F:35])([F:34])[F:33])[O:21][N:20]=[C:19]([C:22]3[CH:30]=[CH:29][C:25]([C:26](Cl)=[O:27])=[C:24]([CH3:31])[CH:23]=3)[CH2:18]2)[CH:13]=[C:14]([Cl:16])[CH:15]=1>N1C=CC=CC=1>[Br:8][C:5]1[CH:4]=[N:3][C:2]([NH:1][C:26](=[O:27])[C:25]2[CH:29]=[CH:30][C:22]([C:19]3[CH2:18][C:17]([C:12]4[CH:13]=[C:14]([Cl:16])[CH:15]=[C:10]([Cl:9])[CH:11]=4)([C:32]([F:35])([F:34])[F:33])[O:21][N:20]=3)=[CH:23][C:24]=2[CH3:31])=[N:7][CH:6]=1

Participants

4

Reactant 2

HCID 2313102-Amino-5-bromopyrimidineHCID 866114794-(5-(3,5-Dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazole-3-yl)-2-methylbenzoyl chloride

Product 1

HCID 86654457HCID 86654457, compoundYield 70%

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Procedure

In a solution of 2.87 g of 2-amino-5-bromopyrimidine in 40 mL of pyridine, 6.00 g of 4-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]-2-methylbenzoyl-chloride synthesized in Step 4 of Synthetic Example 1 was added at room temperature with stirring, and stirred at the same temperature for 2 days. The solvent was distilled off under reduced pressure, the residue was dissolved in 30 mL of 1,4-dioxane, a solution of 3.09 g of potassium hydroxide in 30 mL of water was added and stirred at room temperature for 3 hours. After the completion of the reaction, 20 mL of hydrochloric acid was added in the reaction mixture under cooling with ice and with stirring, extracted with ethyl acetate (50 mL×1), the organic phese was washed with 50 mL of 3N hydrochloric acid, and dehydrated with and dried over saturated sodium chloride aqueous solution and then anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified with neutral alumina column chromatography that was eluated with chloroform to obtain 5.52 g of the aimed product as white crystal.

Workup

  1. stirringstirred at the same temperature for 2 days
  2. distillationThe solvent was distilled off under reduced pressure
  3. dissolutionthe residue was dissolved in 30 mL of 1,4-dioxane
  4. additiona solution of 3.09 g of potassium hydroxide in 30 mL of water was added
  5. stirringstirred at room temperature for 3 hours
  6. customAfter the completion of the reaction, 20 mL of hydrochloric acid
  7. additionwas added in the reaction mixture
  8. temperatureunder cooling with ice
  9. stirringwith stirring
  10. extractionextracted with ethyl acetate (50 mL×1)
  11. washthe organic phese was washed with 50 mL of 3N hydrochloric acid
  12. dry with materialdried over saturated sodium chloride aqueous solution
  13. distillationanhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure
  14. customThe residue was purified with neutral alumina column chromatography that

Sources & evidence

ORD record
ord-d178774167d84da1beaf4e46f9de51c6
Source dataset
uspto-grants-2011_05
Patent number
US07951828B1

Reaction notes

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