HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanimidic acid, ethyl ester, hydrochloride (1:1) → N-((6-chloropyridin-3-yl)methyl)-N-methylethanimidamide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanimidic acid, ethyl ester, hydrochloride (1:1) | HCID 2724290 | — |
| Reactant | 6-Chloro-N-methyl-3-pyridinemethanamine | HCID 11094883 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-((6-chloropyridin-3-yl)methyl)-N-methylethanimidamide hydrochloride | HCID 19967185 | 191.5% |
Reaction Steps
To 40 ml of ethanol was added 5.1 g of N-(2-chloro-5-pyridylmethyl)-N-Methylamine and then 4 g of ethyl acetimidate hydrochloride at 0° C. After stirring for an hour, the reaction mixture was allowed to warm to room temperature and stirred over night. The solvent was then distilled off. The obtained white residue was washed with diethyl ether to afford 7.3 g of the title compound m.p. 192°-197° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05304566 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-f2fdee4c7308435e9c9b9449b0ee2875 |
| Source note | uspto-grants-1994_04 |