Phenylacetyl chloride → HCID 57505538, compound

HRID 2391295Notes

Reaction equation

HRID 2391295 reaction equation
[C:1]1([CH2:7][C:8](Cl)=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[S-:11][C:12]#[N:13].[K+].[NH2:15][C:16]1[CH:17]=[C:18]([CH:35]=[CH:36][CH:37]=1)[O:19][C:20]1[CH:21]=[CH:22][C:23]2[N:24]([CH:26]=[C:27]([NH:29][C:30]([CH:32]3[CH2:34][CH2:33]3)=[O:31])[N:28]=2)[N:25]=1>C(#N)C>[C:1]1([CH2:7][C:8]([NH:13][C:12]([NH:15][C:16]2[CH:17]=[C:18]([CH:35]=[CH:36][CH:37]=2)[O:19][C:20]2[CH:21]=[CH:22][C:23]3[N:24]([CH:26]=[C:27]([NH:29][C:30]([CH:32]4[CH2:34][CH2:33]4)=[O:31])[N:28]=3)[N:25]=2)=[S:11])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

5

Reactant 3

HCID 7679Phenylacetyl chlorideHCID 516872Potassium thiocyanateHCID 57386059N-[6-(3-aminophenoxy)imidazo[1,2-b]pyridazin-2-yl]cyclopropanecarboxamide

Product 1

HCID 57505538HCID 57505538, compoundYield 58.4%

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Conditions

Temperature
60 °C

Procedure

To a solution of phenylacetyl chloride (155 mg, 1.0 mmol) in acetonitrile (20 mL) was added potassium thiocyanate (292 mg, 3.0 mmol), and the mixture was stirred at 60° C. for 3 hr and concentrated under reduced pressure. The residue was diluted with tetrahydrofuran (20 mL). N-[6-(3-Aminophenoxy)imidazo[1,2-b]pyridazin-2-yl]cyclopropanecarboxamide (155 mg, 0.50 mmol) was added to the mixture, and the mixture was stirred at room temperature for 18 hr. The reaction mixture was concentrated under reduced pressure, water was added to the residue and the mixture was extracted with ethyl acetate. The organic layer was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/methanol=100/0→70/30) and precipitated from diisopropyl ether to give the title compound (142 mg, yield 58%) as a white solid.

Workup

  1. concentrationconcentrated under reduced pressure
  2. additionThe residue was diluted with tetrahydrofuran (20 mL)
  3. stirringthe mixture was stirred at room temperature for 18 hr
  4. concentrationThe reaction mixture was concentrated under reduced pressure, water
  5. additionwas added to the residue
  6. extractionthe mixture was extracted with ethyl acetate
  7. concentrationThe organic layer was concentrated under reduced pressure
  8. customthe residue was purified by silica gel column chromatography (ethyl acetate/methanol=100/0→70/30)
  9. customprecipitated from diisopropyl ether

Sources & evidence

ORD record
ord-22617f6eeb5f4a8e908846729e36dddc
Source dataset
uspto-grants-2012_09
Patent number
US08273741B2

Reaction notes

Loading…