HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 3-Bromo-5-(4-(pyrrolidine-1-sulfonyl)phenoxy)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromo-5-hydroxypyridine | HCID 599529 | — |
| Reactant | 1-(4-Fluorobenzenesulfonyl)pyrrolidine | HCID 796578 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 3-Bromo-5-(4-(pyrrolidine-1-sulfonyl)phenoxy)pyridine | HCID 21964095 | 59.1% |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
A mixture of 5-bromo-3-pyridinol (2.61 g, 15 mmol), dimethylacetamide (50 mL), 1-((4-fluorophenyl)sulfonyl)pyrrolidine (5.8 g, 25 mmol) and potassium carbonate (4.1 g, 30 mmol) was heated at 120° C. for 18 h, then cooled to room temperature and concentrated by rotary evaporation. The residue was dissolved in ethyl acetate (200 mL) and the organic phase washed with water (3×100 mL) and brine (100 mL), then dried (MgSO4), filtered and concentrated by rotary evaporation. The crude product was purified by column chromatography, eluting with ethyl acetate/cyclohexane (20/80, v/v). Selected fractions containing the product were concentrated via rotary evaporation to give 3.4 g (59%) of a red solid (m.p. 148° C.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07101896B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-3c5af9c391014883b283a8713acbd156 |
| Source note | uspto-grants-2006_09 |