HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-ethyl-4-methylpyridin-2-amine → HCID 178476385, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-ethyl-4-methylpyridin-2-amine | HCID 18428456 | — |
| Reactant | 2-Imino-4-methylpiperidine acetate | HCID 178475870 | — |
| Product | HCID 178476385 | HCID 178476385 | — |
Reaction Steps
The method of preparation of 2-imino-4-methylpiperidine acetate was used to convert 2-(ethylamino)-4-methylpyridine to the title compound except platinum oxide was used as the catalyst. The analysis of the product, obtained as an oil, was found to be consistent with the proposed structure. MH+=141; 1H NMR (D2O): 3.40-3.10 (m, 2H); 3.00 (q, J=6 Hz, 2H); 2.50-2.40 (m, 1H); 2.10-1.90 (m, 1H); 1.83 (s, 3H); 1.80-1.65 (m, 4H); 1.40-1.20 (m 1H); 1.02 (t, J=6 Hz, 3H); 0.83 (d, J=6 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05854234 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-2362ace83b354d5bab0dcd2fe4c612ae |
| Source note | uspto-grants-1998_12 |