HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloroaniline → methyl(2R)-4-((4-chlorophenyl)amino)-2-cyclohexyl-4-oxobutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloroaniline | HCID 7812 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | (3R)-3-cyclohexyl-4-methoxy-4-oxobutanoic acid | HCID 2734512 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | methyl(2R)-4-((4-chlorophenyl)amino)-2-cyclohexyl-4-oxobutanoate | HCID 68647026 | 94.5% |
Reaction Steps
To a suspension of (3R)-3-cyclohexyl-4-methoxy-4-oxobutanoic acid (0.21 g), 4-chloroaniline (0.13 g) and HOBt (0.23 g) in acetonitrile (10 ml) were added WSC (0.29 g) and N-methylmorpholine (0.10 g), and mixed at room temperature for 15 hours. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in ethyl acetate. The ethyl acetate solution was washed sequentially with an aqueous sodium hydrogen carbonate solution, water, a 5% aqueous citric acid solution and saturated brine, and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain the title compound as a pale brown solid (0.30 g, 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820673B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-6096523440a24c799c599e6733b97686 |
| Source note | uspto-grants-2010_10 |