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Acetic Acid → 5-(3-Bromo-6-methoxyimidazo[1,2-b]pyridazin-2-yl)-2-methylaniline

HRID 539742
Notes
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Reaction equation

HRID 539742 reaction equation
[Br:1][C:2]1[N:6]2[N:7]=[C:8]([O:11][CH3:12])[CH:9]=[CH:10][C:5]2=[N:4][C:3]=1[C:13]1[CH:18]=[CH:17][C:16]([CH3:19])=[C:15]([N+:20]([O-])=O)[CH:14]=1.CC(O)=O>C(O)C.O.[Fe]>[Br:1][C:2]1[N:6]2[N:7]=[C:8]([O:11][CH3:12])[CH:9]=[CH:10][C:5]2=[N:4][C:3]=1[C:13]1[CH:18]=[CH:17][C:16]([CH3:19])=[C:15]([CH:14]=1)[NH2:20]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 2

HCID 176Acetic AcidHCID 680890483-Bromo-6-methoxy-2-(4-methyl-3-nitrophenyl)imidazo[1,2-b]pyridazine

Product 1

HCID 575162685-(3-Bromo-6-methoxyimidazo[1,2-b]pyridazin-2-yl)-2-methylanilineYield 97.6%

Reagents, catalysts & solvents 3

HCID 23925IronCatalystHCID 702EthanolSolvent
HCID 962
Water
Solvent

Conditions

Temperature
80 °C

Procedure

To a stirred solution of 3-bromo-6-methoxy-2-(4-methyl-3-nitrophenyl)imidazo[1,2-b]pyridazine (0.190 g, 0.523 mmol) in ethanol (15 mL) and water (5 mL) containing AcOH (3.13 mmol) is added iron (0.146 g, 2.61 mmol). The reaction mixture is heated at 80° C. for 2 hours, cooled, concentrated under reduced pressure and sat. aqueous NaHCO3 (50 mL) is added. The mixture is extracted with EtOAc (3×25 mL). Organic layer is collected, dried over Na2SO4, filtered and concentrated to dryness. The crude product is purified via chromatography using a gradient of hexanes to EtOAc to afford the title compound (0.170 g, 89%) as an off-white solid: Rf 0.18 (1:1 EtOAc:hexanes); LCMS (m/z)=333.2, 335.2 [M+H]+, tR=2.22 min.

Workup

  1. temperaturecooled
  2. concentrationconcentrated under reduced pressure and sat. aqueous NaHCO3 (50 mL)
  3. additionis added
  4. extractionThe mixture is extracted with EtOAc (3×25 mL)
  5. customOrganic layer is collected
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated to dryness
  9. customThe crude product is purified via chromatography

Sources & evidence

ORD record
ord-ce246f9323184c2e862fbbe6de44cfad
Source dataset
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08871767B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes