HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-[2-[(4-Methyl-2-pyridyl)amino]ethyl]methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | N-(4-methylpyridin-2-yl)ethane-1,2-diamine | HCID 10034794 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[2-[(4-Methyl-2-pyridyl)amino]ethyl]methanesulfonamide | HCID 61724432 | 101.1% |
Reaction Steps
To a cooled (0° C.) solution of N-(4-methyl-2-pyridyl)ethane-1,2-diamine (683 mg, 4.52 mmol) in dichloromethane (25 ml) were added triethyl amine (1.26 ml, 9.06 mmol) followed by methanesulfonyl chloride (370 μl, 4.78 mmol). The mixture was stirred at room temperature for two hours and washed with saturated sodium bicarbonate solution. The organic phase was dried over sodium sulfate and concentrated to give 1.04 g of a yellow oil (4.57 mmol, 95%) MS(ESI) m/z=230.1 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09321724B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-df98dda310a04dda97802fd56cae038a |
| Source note | uspto-grants-2016_04 |