HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 3-[{[4-({Cyclohexyl[3-methyl-5-(pyridin-2-ylmethoxy)-1-benzofuran-2-yl]methyl}amino)phenyl]carbonyl}(methyl)amino]propanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 3-[{[4-({cyclohexyl[3-methyl-5-(pyridin-2-ylmethoxy)-1-benzofuran-2-yl]methyl}amino)phenyl]carbonyl}(methyl)amino]propanoate | HCID 66778018 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-[{[4-({Cyclohexyl[3-methyl-5-(pyridin-2-ylmethoxy)-1-benzofuran-2-yl]methyl}amino)phenyl]carbonyl}(methyl)amino]propanoic acid | HCID 68628398 | 60.8% |
Reaction Steps
Ethyl 3-[{[4-({cyclohexyl[3-methyl-5-(pyridin-2-ylmethoxy)-1-benzofuran-2-yl]methyl}amino)phenyl]carbonyl}(methyl)amino]propanoate (0.19 g) synthesized in the above-mentioned (2) was dissolved in ethanol (5 mL), 1N aqueous sodium hydroxide solution (1.0 mL) was added to the solution at room temperature, and the mixture was stirred at room temperature for 0.5 hr. Ethanol was evaporated under reduced pressure, 1N hydrochloric acid (1.0 mL) was added to the residue, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was washed with ethanol-water to give the title object compound (0.11 g, 41%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08436043B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-d464041478f344328adac895b829c95c |
| Source note | uspto-grants-2013_05 |