HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Tert-butyl (1-(methylsulfonyl)piperidin-3-yl)methylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | tert-butyl N-[(piperidin-3-yl)methyl]carbamate | HCID 2756030 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl (1-(methylsulfonyl)piperidin-3-yl)methylcarbamate | HCID 47411127 | — |
Reaction Steps
tert-Butyl piperidin-3-ylmethylcarbamate (500 mg) was dissolved in anhydrous dichloromethane (10 mL), and methanesulfonyl chloride (0.181 mL) was added followed by the addition of triethylamine (1.3 mL). The reaction mixture was stirred at room temperature overnight. The organic solvent was removed under vacuum. The residue was purified with flash column chromatography on silica gel eluting with 0-70% ethyl acetate in hexane to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09045475B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-56d92eb8868548be83e7c69ffd25d95a |
| Source note | uspto-grants-2015_06 |