HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (1-(4-Methylpyridin-2-yl)piperidin-4-yl)methyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (1-(4-Methylpyridin-2-yl)piperidin-4-yl)methanol | HCID 61725157 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (1-(4-Methylpyridin-2-yl)piperidin-4-yl)methyl methanesulfonate | HCID 86673349 | — |
Reaction Steps
(1-(4-Methylpyridin-2-yl)piperidin-4-yl)methanol (0.970 mmol, 0.2 g) and triethylamine (2.91 mmol, 0.404 mL, 0.294 g) were stirred in DCM at 0° C. Methanesulfonyl chloride (1.454 mmol, 0.113 mL, 0.167 g) was added dropwise and the reaction allowed to warm to room temperature and stirred for 1 hour. The reaction mixture was washed with water, dried over Na2SO4 and concentrated in vacuo to afford (1-(4-methylpyridin-2-yl)piperidin-4-yl)methyl methanesulfonate. (0.234 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09115126B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-bf002950ef5f45cfb2ee204857de9227 |
| Source note | uspto-grants-2015_08 |