HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717237Generated: November 3, 2026
Triethylamine → N-cyclopropyl-1-{4-[(N,N-dimethylglycyl)amino]phenyl}-5-propyl-1H-1,2,3-triazole-4-carboxamide
https://huagongshe.com/reaction/1717237
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1-(4-aminophenyl)-N-cyclopropyl-5-propyl-1H-1,2,3-triazole-4-carboxamide | HCID 68517548 | — |
| Catalyst | N,N-Dimethylglycine hydrochloride | HCID 75605 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-cyclopropyl-1-{4-[(N,N-dimethylglycyl)amino]phenyl}-5-propyl-1H-1,2,3-triazole-4-carboxamide | HCID 68511935 | 24% |
Reaction Steps
To a solution of N,N-dimethylglycine hydrochloride (0.17 mg), triethylamine (0.17 ml) and HOBt (0.18 g) in dichloromethane (10 ml) was added WSC (0.23 g), and the mixture was stirred at room temperature for 20 min. 1-(4-Aminophenyl)-N-cyclopropyl-5-propyl-1H-1,2,3-triazole-4-carboxamide (0.29 g) obtained in Example 1d) was added to the reaction mixture, and the mixture was stirred at room temperature for 3 days. The reaction mixture was diluted with dichloromethane, and washed with aqueous sodium hydrogen carbonate solution. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by high performance liquid chromatography to give the title compound as a white powder (0.09 g, 24%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07803822B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-5631716c378e46b39f480bfad479c940 |
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| Source note | uspto-grants-2010_09 |
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