HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Bisegliptin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (2S,4S)-1-[2-(benzenesulfonyloxy)acetyl]-4-fluoropyrrolidine-2-carbonitrile | HCID 24781881 | — |
| Reactant | Ethyl 4-aminobicyclo[2.2.2]octane-1-carboxylate hydrobromide | HCID 67053432 | — |
| Solvent | Water | HCID 962 | — |
| Product | Bisegliptin | HCID 11688894 | 83% |
Reaction Steps
Ethyl 4-aminobicyclo[2.2.2]octane-1-carboxylate hydrobromide (612 mg), potassium carbonate (608 mg) and N,N-dimethylformamide (4 mL) were mixed together. To this mixture, (2S,4S)-4-fluoro-1-[2-(benzenesulfonyloxy)acetyl]pyrrolidine-2-carbonitrile (625 mg) was added at 40° C. and the mixture was further stirred for 1 hour. Subsequently, water (10 mL) was added and the resulting crystal was collected by filtration. This product was washed with water (5 mL) and dried at 50° C. under reduced pressure to give (2S,4S)-1-[2-[(4-ethoxycarbonylbicyclo[2.2.2]oct-1-yl)amino]ac etyl]-4-fluoropyrrolidine-2-carbonitrile as a colorless powder (581 mg, 83% yield). This compound was identical to the compound obtained in Example 7.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915427B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-80028d8024e1440faf5b2a5996d4929a |
| Source note | uspto-grants-2011_03 |