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 | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Chloro-N-(2,6-diisopropylphenyl)acetamide | HCID 2363774 | — |
| Reactant | (1-Amino-methylcyclohexyl)phenylamine | HCID 68630087 | — |
| Product | N-(2,6-diisopropylphenyl)-2-[(1-phenylamino-cyclohexylmethyl)amino]acetamide | HCID 25227156 | 71% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
340 mg (1.34 mmol) of 2-chloro-N-(2,6-diisopropylphenyl)acetamide (obtained in Example 3/c) are added to 270 mg (1.32 mmol) of (1-amino-methylcyclohexyl)phenylamine (obtained in Example 2/b) 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 and then dried over sodium sulfate. The solvents are evaporated. The residue is chromatographed on silica gel (heptane/ethyl acetate 80/20, v/v). 396 mg of N-(2,6-diisopropylphenyl)-2-[(1-phenylaminocyclohexylmethyl)-amino]acetamide are obtained in the form of a white solid. M.p. 104-6° C., yield=71%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08513307B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-a98c3384440c460fb1311e685c759ecf |
| Source note | uspto-grants-2013_08 |