HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → (+/-)-(5-Nitro-2,4,6,7-tetramethyldihydrobenzofuran-2-yl)-[4-(4-1h-pyrazol-5-ylphenyl)-piperazin-1-yl]carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HOBT hydrochloride | HCID 22729017 | — |
| Reactant | 1-(4-1H-pyrazol-5-ylphenyl)-piperazine | HCID 23118309 | — |
| Reactant | 2,4,6,7-Tetramethyl-5-nitrodihydrobenzofuran-2-carboxylic acid | HCID 68844454 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | (+/-)-(5-Nitro-2,4,6,7-tetramethyldihydrobenzofuran-2-yl)-[4-(4-1h-pyrazol-5-ylphenyl)-piperazin-1-yl]carboxamide | HCID 68845480 | 90.6% |
Reaction Steps
To 0.38 g of 1-(4-1H-pyrazol-5-ylphenyl)-piperazine and 0.4 g of 2,4,6,7-tetramethyl-5-nitrodihydrobenzofuran-2-carboxylic acid, 0.35 g of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, 0.25 g of 1-hydroxybenzotriazole hydrochloride and 0.19 g of triethylamine were added, followed by stirring at room temperature for 24 hours. The reaction solution was poured into water and the precipitated crystal was removed by filtration and washed with water, and then the resulting crystal was dried to obtain 0.65 g of the objective compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07553837B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-41996fa04e8343d4bc13a543273b67dc |
| Source note | uspto-grants-2009_06 |