HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2-(4-Phenyl-2-(piperidin-1-yl)-6-p-tolylpyrimidin-5-yl)pentanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 2-(4-phenyl-2-(piperidin-1-yl)-6-p-tolylpyrimidin-5-yl)pentanoate | HCID 66955993 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(4-Phenyl-2-(piperidin-1-yl)-6-p-tolylpyrimidin-5-yl)pentanoic acid | HCID 66955862 | 68.1% |
Reaction Steps
This compound was prepared according to general method D from methyl-2-(4-phenyl-2-(piperidin-1-yl)-6-p-tolylpyrimidin-5-yl)pentanoate (0.018 g; 0.041 mmol), sodium hydroxide 5N (0.100 mL; 0.50 mmol) in methanol (1 mL) at 60° C. for 72 h. The reaction mixture was concentrated under reduced pressure, the residue was dissolved in water and extracted with diethyl ether. The pH of the aqueous layer was adjusted between 2 and 3 by addition of a solution of hydrochloric acid 6N until a precipitate was formed. The suspension was extracted twice with ethyl acetate and the combined organic layers were dried over sodium sulfate and concentrated under reduced pressure to give 0.012 g (68%)of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08906906B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-9fbfc520a1d84e24b93efec8ace88d58 |
| Source note | uspto-grants-2014_12 |