HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ether hydrochloride → Evogliptin hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ether hydrochloride | HCID 10953452 | — |
| Reactant | HCID 86641589 | HCID 86641589 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Evogliptin hydrochloride | HCID 25022353 | — |
Reaction Steps
97 mg of tert-butyl (R)-4-[(R)-2-(tert-butoxymethyl)-3-oxopiperazin-1-yl]-4-oxo-1-(2,4,5-trifluorophenyl)butan-2-ylcarbamate prepared in Step 8 was dissolved in 3 mL of methanol, followed by addition of 2 mL of 2N-hydrochloric acid/diethyl ether and stirring at room temperature for 3 hours. The reaction mixture was concentrated and dried under reduced pressure to afford 64 mg of the title compound as a foamy solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08030315B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-3f10e5fc5ef445cc8fdbf936612c772e |
| Source note | uspto-grants-2011_10 |