HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-(2,6-diisopropylphenyl)-2-[(1-phenylamino-cyclohexylmethyl)amino]acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Chloro-N-(2,6-diisopropylphenyl)acetamide | HCID 2363774 | — |
| Reactant | N-[1-(Aminomethyl)cyclohexyl]aniline | HCID 16227755 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(2,6-diisopropylphenyl)-2-[(1-phenylamino-cyclohexylmethyl)amino]acetamide | HCID 25227156 | 56.1% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
620 mg (2.45 mmol) of 2-chloro-N-(2,6-diisopropylphenyl)acetamide are added to 500 mg (2.45 mmol) of (1-aminomethylcyclohexyl)phenylamine in 10 ml of dimethylformamide. The reaction medium is stirred at 100° C. under microwave irradiation for 30 min. It is then poured into water and extracted with ethyl acetate. The organic phases are collected and washed with water. They are dried over sodium sulfate. The solvents are evaporated. The residue is chromatographed on silica gel (heptane/ethyl acetate 80/20, v/v). 580 mg of N-(2,6-diisopropylphenyl)-2-[(1-phenylaminocyclohexyl-methyl)amino]acetamide are obtained in the form of a beige solid. Yield=56%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08513307B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-cc114cb2a6984066ae3304e889bbe4ff |
| Source note | uspto-grants-2013_08 |