HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 5-Bromo-2-((S)-3-fluoro-pyrrolidin-1-yl)-nicotinonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (s)-3-Fluoropyrrolidine hydrochloride | HCID 16217739 | — |
| Reactant | 5-Bromo-2-chloronicotinonitrile | HCID 21948269 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-Bromo-2-((S)-3-fluoro-pyrrolidin-1-yl)-nicotinonitrile | HCID 90356697 | — |
Reaction Steps
5-Bromo-2-chloro-nicotinonitrile (6) (5.0 g, 23.0 mmol) was dissolved in MeCN (100 mL). (S)-3-Fluoropyrrolidine hydrochloride (5.7 g, 53.0 mmol) and DIPEA (12.0 mL, 68.9 mmol) were added and the mixture was stirred at reflux for 1 hour. The solvent was evaporated in vacuo and the residue partitioned between EtOAc (100 mL) and H2O (50 mL). The layers were separated and the organic phase washed with saturated brine solution (50 mL), then dried (MgSO4), filtered and the solvent evaporated in vacuo. The title compound was obtained as an off-white solid (6.2 g, 100%); LCMS, Rt=2.91 min (MeOH-FA method), m/z 270, 272 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09433622B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-959ad8dfe6724d83b24fbb5c45a759ae |
| Source note | uspto-grants-2016_09 |