N-bromobutanimide → 5-Bromo-2,6-Diamino-3-(2,3,5-trichlorophenyl)pyrazine

HRID 1358982Notes

Reaction equation

HRID 1358982 reaction equation
[Br:1]N1C(=O)CCC1=O.[NH2:9][C:10]1[C:15]([C:16]2[CH:21]=[C:20]([Cl:22])[CH:19]=[C:18]([Cl:23])[C:17]=2[Cl:24])=[N:14][CH:13]=[C:12]([NH2:25])[N:11]=1>CS(C)=O.O>[Br:1][C:13]1[N:14]=[C:15]([C:16]2[CH:21]=[C:20]([Cl:22])[CH:19]=[C:18]([Cl:23])[C:17]=2[Cl:24])[C:10]([NH2:9])=[N:11][C:12]=1[NH2:25]

Participants

5

Conditions

Temperature
15 °C

Procedure

N-Bromosuccinimide (0.194 g, 1.09×10−3 mole) was added over 20 min to a mixture of 2,6-Diamino-3-(2,3,5-trichlorophenyl)pyrazine (0.3 g, 1.04×10−3 mole) in dimethylsulfoxide (10 ml) and water (0.25 ml) below 15° C. The resulting reaction mixture was stirred at 15° C. for 1 hr, poured onto ice water (150 ml) and extracted with ethyl acetate (2×75 ml). The extract was then washed with 2 M sodium carbonate solution (50 ml) and water (100 ml), dried over anhydrous magnesium sulphate, filtered and the filtrate evaporated in vacuo. The residue was purified by ‘flash chromatography’ using 5-13% ethyl acetate in cyclohexane as the eluent. Yield 0.183 g (48%), M.p. 222-224° C.

Workup

  1. customThe resulting reaction mixture
  2. additionpoured onto ice water (150 ml)
  3. extractionextracted with ethyl acetate (2×75 ml)
  4. washThe extract was then washed with 2 M sodium carbonate solution (50 ml) and water (100 ml)
  5. dry with materialdried over anhydrous magnesium sulphate
  6. filtrationfiltered
  7. customthe filtrate evaporated in vacuo
  8. customThe residue was purified by ‘flash chromatography’

Sources & evidence

ORD record
ord-956f0b83539e43a98798bfb4e8e59295
Source dataset
uspto-grants-2003_07
Patent number
US06599905B2

Reaction notes

Loading…