HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (S)-2-[5-Naphthalen-1-yl-2-oxo-3-(4-trifluoromethylbenzoylamino)-2H-pyridin-1-yl]-3-phenylpropionic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | (S)-2-[5-Naphthalen-1-yl-2-oxo-3-(4-trifluoromethylbenzoylamino)-2H-pyridin-1-yl]-3-phenylpropionic acid methyl ester | HCID 69587926 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-2-[5-Naphthalen-1-yl-2-oxo-3-(4-trifluoromethylbenzoylamino)-2H-pyridin-1-yl]-3-phenylpropionic acid | HCID 58680180 | — |
Reaction Steps
A mixture of (S)-2-[5-naphthalen-1-yl-2-oxo-3-(4-trifluoromethyl-benzoylamino)-2H-pyridin-1-yl]-3-phenylpropionic acid methyl ester from Step F (31 mg, 0.054 mmol) and 1N lithium hydroxide (2.0 mL) in tetrahydrofuran (2.0 mL) was stirred at room temperature for 1 h. 1N Hydrochloric acid (3 mL) was added and the mixture was extracted with dichloromethane (3×10 mL). The combined organic layer was dried with sodium sulfate, filtered and concentrated in vacuo to give a quantitative yield of the title compound. MS 557.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07087622B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-2bc70584fccd43939cccf6094ec7e59c |
| Source note | uspto-grants-2006_08 |