1,1'-Carbonyldiimidazole → 3-methyl-3H-benzotriazole-5-carboxylic acid methoxy-methyl-amide

HRID 1868334Notes

Reaction equation

HRID 1868334 reaction equation
[CH3:1][N:2]1[C:6]2[CH:7]=[C:8]([C:11]([OH:13])=O)[CH:9]=[CH:10][C:5]=2[N:4]=[N:3]1.C(N1C=CN=C1)(N1C=CN=C1)=O.Cl.[CH3:27][NH:28][O:29][CH3:30]>CN(C)C=O>[CH3:30][O:29][N:28]([CH3:27])[C:11]([C:8]1[CH:9]=[CH:10][C:5]2[N:4]=[N:3][N:2]([CH3:1])[C:6]=2[CH:7]=1)=[O:13]

Participants

5

Procedure

3-Methyl-3H-benzotriazole-5-carboxylic acid (1.67 g, 5.6 mmol) was suspended in 25 ml N,N-dimethylformamide. 1,1′-carbonyldiimidazole (1.0 g, 6.2 mmol) was added and the reaction stirred at room temperature for 90 minutes. Then, N,O-dimethylhydroxylamine hydrochloride (593 mg, 6.2 mmol) was added and the reaction stirred at room temperature overnight. The solvent was removed by rotary evaporation. The residue was dissolved in saturated aqueous ammonium chloride solution and extracted three times with chloroform. The combined organics were dried over sodium sulfate, filtered and concentrated to dryness. Crude material was purified on Biotage Flash 40S silica gel column using chloroform/methanol gradient system (100:0 to 97:3, respectively) as eluent to afford 3-methyl-3H-benzotriazole-5-carboxylic acid methoxy-methyl-amide (1.0 g, 82%).

Workup

  1. stirringthe reaction stirred at room temperature overnight
  2. customThe solvent was removed by rotary evaporation
  3. dissolutionThe residue was dissolved in saturated aqueous ammonium chloride solution
  4. extractionextracted three times with chloroform
  5. dry with materialThe combined organics were dried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated to dryness
  8. customCrude material was purified on Biotage Flash 40S silica gel column

Sources & evidence

ORD record
ord-fce8b74d64be4809b7bba699c5c64490
Source dataset
uspto-grants-2009_12
Patent number
US07635702B2

Reaction notes

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