HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methylethylamine → N-[2-(3-cyanophenoxy)ethyl]-4-(N-methyl-N-ethylcarbamoyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methylethylamine | HCID 12219 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 4-[N-[2-(3-cyanophenoxy)ethyl]carbamoyl]benzoic acid | HCID 68831518 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | N-[2-(3-cyanophenoxy)ethyl]-4-(N-methyl-N-ethylcarbamoyl)benzamide | HCID 68830104 | — |
Reaction Steps
258 mg (0.83 mmol) of 4-[N-[2-(3-cyanophenoxy)ethyl]carbamoyl]benzoic acid, 53 mg (0.9 mmol) of N-ethyl-N-methylamine, 129 mg (0.83 mmol) of 1-hydroxybenzotriazole (hydrous, 87%) and 159 mg (0.83 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride were stirred in 10 ml of dichloro ee at room temperature overnight. The resultant mixture was diluted with 1 N hydrochloric acid. After the extraction with dichloromethane, the organic layer was washed with 1 N aqueous sodium hydroxide solution and then with saturated aqueous NaCl solution and dried over anhydrous magnesium-sulfate. The solvent was evaporated to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07396844B1 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-e3b794dff0b24d9bb6be2ed2c9b71621 |
| Source note | uspto-grants-2008_07 |