Hydrochloric Acid → 7-bromo-2-methyl-3H-benzo[d]imidazol-5-amine

HRID 1622440Notes

Reaction equation

HRID 1622440 reaction equation
[Br:1][C:2]1[C:10]2[N:9]=[C:8]([CH3:11])[NH:7][C:6]=2[CH:5]=[C:4]([N+:12]([O-])=O)[CH:3]=1.O.O.[Sn](Cl)Cl.Cl>CO>[Br:1][C:2]1[C:10]2[N:9]=[C:8]([CH3:11])[NH:7][C:6]=2[CH:5]=[C:4]([NH2:12])[CH:3]=1

Participants

5

Conditions

Temperature
65 °C

Procedure

To a solution of 4-bromo-2-methyl-6-nitro-1H-benzo[d]imidazole (35 g, 137 mmol) and Tin(II) chloride dihydrate (185 g, 822 mmol) in methanol (800 mL) was added conc. HCl (10 mL), and the mixture was stirred at 65° C. for 2 h. Then the solvent was removed in vacuo, and the residue was diluted with 1N Na2CO3 solution (600 mL) and extracted with ethyl acetate (500 mL×3). The combined organic layers were washed with brine, dried over sodium sulphate and evaporated to give the crude product (30.2 g, 97%) as a brown solid; LC/MS: MS (ES+) m/e 226 [M+H]+; 1H NMR (300 MHz, DMSO-d6) δ ppm 2.38 (s, 3H), 4.98 (s, 2H), 6.52 (d, J=1.5 Hz, 1H), 6.66 (d, J=1.5 Hz, 1H), 11.86 (s, br, 1H).

Workup

  1. customThen the solvent was removed in vacuo
  2. additionthe residue was diluted with 1N Na2CO3 solution (600 mL)
  3. extractionextracted with ethyl acetate (500 mL×3)
  4. washThe combined organic layers were washed with brine
  5. dry with materialdried over sodium sulphate
  6. customevaporated

Sources & evidence

ORD record
ord-c5f8509a470347b780a3ba6e991d1202
Source dataset
uspto-grants-2014_07
Patent number
US08778937B2

Reaction notes

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