HuagongsheHuagongshe Chemistry Print Report · For research reference only
Betahistine → HCID 13822937, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Betahistine | HCID 2366 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 13822937 | HCID 13822937 | — |
Reaction Steps
Acryloyl chloride (4.52 g, 0.05 mole) was added dropwise to a stirring solution of triethylamine (30 ml) and 2-(β-methylaminoethyl)pyridine (6.81 g, 0.05 mole) in ethyl ether (500 ml). After stirring overnight at room temperature, the white solid was removed by filtration and washed well with ethyl ether. The organic phases were combined, dried over sodium sulfate, filtered then concentrated to dryness to give an orange oil. The structure was confirmed by NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05189038 |
| Source dataset | uspto-grants-1993_02 |
| ORD ID | ord-dfc60474c6fc4d5385697d931541882e |
| Source note | uspto-grants-1993_02 |