HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl cyanoacetate → 2-(1-ethyl-1H-imidazo[4,5-c]pyridin-2-yl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl cyanoacetate | HCID 7764 | — |
| Reactant | 4-N-ethylpyridine-3,4-diamine | HCID 12036392 | — |
| Product | 2-(1-ethyl-1H-imidazo[4,5-c]pyridin-2-yl)acetonitrile | HCID 46835262 | 37.3% |
Reaction Steps
The product from Step 2 (500 mg, 3.6 mmole) and ethyl cyanoacetate (620 mg, 5.5 mmol) were heated together at 190° C. for 20 minutes. After cooling to room temperature, the residue was purified by column chromatography eluting with 10% methanol in ethyl acetate to afford the title compound (250 mg, 37%); MS (ES+) m/e 187 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07348339B2 |
| Source dataset | uspto-grants-2008_03 |
| ORD ID | ord-ebcc45573a904d45bc1b6c093e6679a4 |
| Source note | uspto-grants-2008_03 |