HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (5-Bromo-3-fluoropyridin-2-yl)methyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (5-Bromo-3-fluoropyridin-2-yl)methanol | HCID 57416937 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (5-Bromo-3-fluoropyridin-2-yl)methyl methanesulfonate | HCID 86668676 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
(5-Bromo-3-fluoropyridin-2-yl)methanol (0.20 g, 0.99 mmol) was dissolved in dichloromethane (5 mL), cooled to 0° C. and treated with triethylamine (0.15 mL, 1.1 mmol, 1.1 equiv) and methanesulfonyl chloride (0.085 mL, 1.1 mmol, 1.1 equiv). After 15 minutes, the mixture was diluted with dichloromethane (100 mL) and washed once with sodium bicarbonate (20 mL, aqueous saturated) and brine (50 mL), dried with sodium sulfate, filtered and concentrated in vacuo, providing the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08895580B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-66f59257680747539b5e9c98e033cd70 |
| Source note | uspto-grants-2014_11 |