HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide diethylacetal → ethyl 3-(dimethylamino)-2-(2-oxopyridin-1(2H)-yl)acrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide diethylacetal | HCID 70913 | — |
| Reactant | Ethyl 2-(2-oxopyridin-1-YL)acetate | HCID 9497629 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | ethyl 3-(dimethylamino)-2-(2-oxopyridin-1(2H)-yl)acrylate | HCID 131732878 | 85% |
Reaction Steps
Combined ethyl 2-(2-oxopyridin-1(2H)-yl)acetate (500 mg, 2.76 mmol), 1,1-diethoxy-N,N-dimethylmethanamine (2031 mg, 13.80 mmol) and DMF (2 mL) and heated at 100° C. for 15 h. The reaction mixture was diluted with xylenes and concentrated onto Celite® then purified on a 30 g NH silica column (Moritex) eluted with 0 to 100% EtOAc in hexanes to give the title compound (551 mg, 85% yield) as a light yellow solid. MS m/z 237 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.13 (br. s., 3H) 2.77 (br. s., 6H) 3.94-4.08 (m, 2H) 6.17 (td, J=6.7, 1.3 Hz, 1H) 6.36 (dt, J=9.0, 1.1 Hz, 1H) 7.35-7.45 (m, 2H) 7.47 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09345713B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-db811c5c6ace4f30804bd6c93ca090fe |
| Source note | uspto-grants-2016_05 |