Bromine → HCID 71819024, compound

HRID 1097487Notes

Reaction equation

HRID 1097487 reaction equation
[S-:1][C:2]#[N:3].[K+].[NH2:5][C:6]1[CH:26]=[CH:25][C:9]([O:10][C:11]2[CH:12]=[CH:13][C:14]([F:24])=[C:15]([NH:17][C:18](=[O:23])[C:19]([F:22])([F:21])[F:20])[CH:16]=2)=[C:8]([C:27]#[N:28])[CH:7]=1.BrBr>C(O)(=O)C>[NH2:3][C:2]1[S:1][C:7]2[C:8]([C:27]#[N:28])=[C:9]([O:10][C:11]3[CH:12]=[CH:13][C:14]([F:24])=[C:15]([NH:17][C:18](=[O:23])[C:19]([F:21])([F:20])[F:22])[CH:16]=3)[CH:25]=[CH:26][C:6]=2[N:5]=1

Participants

5

Reactant 3

HCID 24408BromineHCID 516872Potassium thiocyanateHCID 71819023HCID 71819023, compound

Product 1

HCID 71819024HCID 71819024, compoundYield 85.1%

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent3×

Procedure

Potassium thiocyanate (7.72 g, 79.4 mmol) was suspended in acetic acid (30 mL), and the suspension was stirred at room temperature for 10 min. A solution of N-[5-(4-amino-2-cyanophenoxy)-2-fluorophenyl]-2,2,2-trifluoroacetamide (5.4 g, 15.9 mmol) in acetic acid (200 mL) was added to the obtained solution, and the mixture was further stirred at room temperature for 10 min. A solution of bromine (5.05 g, 31.5 mmol) in acetic acid (30 mL) was slowly added dropwise to the obtained solution. After the completion of the dropwise addition, the mixture was stirred at room temperature for 12 hr. The resulting yellow insoluble material was filtered off and washed with acetic acid. The filtrate and washings were combined and the mixture was concentrated under reduced pressure. The obtained residue was suspended in ethyl acetate (500 ml), washed successively with saturated aqueous sodium hydrogen carbonate solution (250 mL×2) and saturated brine (250 mL), and dried over anhydrous sodium sulfate. Insoluble material was filtered off, and the filtrate was purified by silica gel column chromatography (eluate: ethyl acetate). The obtained solution was concentrated under reduced pressure to give the title compound (5.36 g, 85%) as a pale-yellow powder.

Workup

  1. stirringthe mixture was further stirred at room temperature for 10 min
  2. additionAfter the completion of the dropwise addition
  3. stirringthe mixture was stirred at room temperature for 12 hr
  4. filtrationThe resulting yellow insoluble material was filtered off
  5. washwashed with acetic acid
  6. concentrationthe mixture was concentrated under reduced pressure
  7. washwashed successively with saturated aqueous sodium hydrogen carbonate solution (250 mL×2) and saturated brine (250 mL)
  8. dry with materialdried over anhydrous sodium sulfate
  9. filtrationInsoluble material was filtered off
  10. customthe filtrate was purified by silica gel column chromatography (eluate: ethyl acetate)
  11. concentrationThe obtained solution was concentrated under reduced pressure

Sources & evidence

ORD record
ord-ee23293fd81243b0bec9e99d16c152e3
Source dataset
uspto-grants-2012_03
Patent number
US08143258B2

Reaction notes

Loading…