HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860100Generated: October 28, 2026
1,1'-Carbonyldiimidazole → 3-methyl-3H-benzotriazole-5-carboxylic acid methoxy-methyl-amide
https://huagongshe.com/reaction/860100
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | 1-methyl-1H-1,2,3-benzotriazole-6-carboxylic acid | HCID 17836426 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-methyl-3H-benzotriazole-5-carboxylic acid methoxy-methyl-amide | HCID 85957172 | 82% |
Reaction Steps
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 (1.01 g, 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07153872B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-9fce7cc8ae9d49d881d744b77a11d1ed |
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| Source note | uspto-grants-2006_12 |
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