N-bromobutanimide → 6-(4-Bromo-phenylamino)-7-chloro-3H-benzoimidazole-5-carboxylic acid methyl ester

HRID 217073Notes

Reaction equation

HRID 217073 reaction equation
[CH3:1][O:2][C:3]([C:5]1[C:13]([NH:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[C:12]([Cl:21])[C:8]2[N:9]=[CH:10][NH:11][C:7]=2[CH:6]=1)=[O:4].C1C(=O)N([Br:29])C(=O)C1>CN(C=O)C>[CH3:1][O:2][C:3]([C:5]1[C:13]([NH:14][C:15]2[CH:16]=[CH:17][C:18]([Br:29])=[CH:19][CH:20]=2)=[C:12]([Cl:21])[C:8]2[N:9]=[CH:10][NH:11][C:7]=2[CH:6]=1)=[O:4]

Participants

4

Procedure

7-Chloro-6-phenylamino-3H-benzoimidazole-5-carboxylic acid methyl ester 7c (0.327 g, 1.08 mmol) is dissolved into DMF (16 mL) and NBS (0.193 g, 1.08 mmol) is added. After one hour, the reaction mixture is quenched by the addition of saturated aqueous NaHSO3. The reaction mixture is then partitioned between EtOAc/THF and water. The organic layer is washed with water and brine. The combined organic extracts are dried (Na2SO4) and concentrated under reduced pressure. The recovered solid is triturated with ether to give 0.225 g (54%) pure desired product. MS ESI (+) m/z 382, 384 (M+, Br pattern) detected.

Workup

  1. additionis added
  2. customthe reaction mixture is quenched by the addition of saturated aqueous NaHSO3
  3. customThe reaction mixture is then partitioned between EtOAc/THF and water
  4. washThe organic layer is washed with water and brine
  5. dry with materialThe combined organic extracts are dried (Na2SO4)
  6. concentrationconcentrated under reduced pressure
  7. customThe recovered solid is triturated with ether

Sources & evidence

ORD record
ord-481fb1765ed84a35ad29fc79b53476d4
Source dataset
uspto-grants-2012_06
Patent number
US08193231B2

Reaction notes

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