Sodium Carbonate → 3-Amino-4-bromo-6-chloropyridazine

HRID 1051756Notes

Reaction equation

HRID 1051756 reaction equation
[Cl:1][C:2]1[N:7]=[N:6][C:5]([NH2:8])=[CH:4][CH:3]=1.C(=O)([O-])[O-].[Na+].[Na+].[Br:15]Br>CO>[Br:15][C:4]1[CH:3]=[C:2]([Cl:1])[N:7]=[N:6][C:5]=1[NH2:8]

Participants

5

Procedure

To a stirred mixture of 6-chloropyridazin-3-amine (D-1) (52.0 g, 0.4 mol, 1.0 eq) and sodium carbonate (84.8 g, 0.8 mol, 2.0 eq) in MeOH (500 mL) at RT, bromine (70.6 g, 0.44 mol, 1.1 eq) is added dropwise and the resulting mixture is stirred overnight. The reaction mixture is filtered and the filter cake is washed with ethyl acetate. The filtrate is concentrated in vacuo and the residue is poured into water (300 mL). The resulting mixture is extracted with ethyl acetate (2×300 mL). The combined organic layers are dried over Na2SO4 and filtered. The filtrate is concentrated in vacuo and the residue is purified by flash column chromatography on silica gel (0-50% ethyl acetate-petroleum ether) to afford the product, 4-bromo-6-chloropyridazin-3-amine (D-2).

Workup

  1. filtrationThe reaction mixture is filtered
  2. washthe filter cake is washed with ethyl acetate
  3. concentrationThe filtrate is concentrated in vacuo
  4. additionthe residue is poured into water (300 mL)
  5. extractionThe resulting mixture is extracted with ethyl acetate (2×300 mL)
  6. dry with materialThe combined organic layers are dried over Na2SO4
  7. filtrationfiltered
  8. concentrationThe filtrate is concentrated in vacuo
  9. customthe residue is purified by flash column chromatography on silica gel (0-50% ethyl acetate-petroleum ether)

Sources & evidence

ORD record
ord-b3de5c06447e4ab28d3fe0eecbe9ccb6
Source dataset
uspto-grants-2016_07
Patent number
US09388183B2

Reaction notes

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