Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Ethyl 2-cyano-4,4-diethoxybutyrate | HCID 4151505 | — |
| Reactant | HCID 135741896 | HCID 135741896 | — |
| Product | HCID 178433412 | HCID 178433412 | — |
Reaction Steps
Acetamidine hydrochloride (2, 0.05 mol, 4.7 g) was added to the 0.1 M sodium ethoxide solution (75 ml) and kept stirring under room temperature for 0.5 h. After removing the formed sodium chloride by filtration, the filtrate was added the ethyl α-cyano-γ,γ-diethoxybutyrate (1, 0.05 mol, 11.5 g) and the solution was heated under reflux for 5 h. After the removal of most solvent under vacuum, acetic acid was added to adjust the pH to 7.0 and 10.8 g precipitation as white powder. Ethanol (110 ml) with concentrated sulfuric acid (2 ml) was added to the collected powder and was refluxed for 2 h. By the end of the reaction an equal volume of water was added and kept at 4° C. overnight. The pyrrolopyrimidine 3 precipitated as white powder (2.1 g) was used for next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08946239B2 |
|---|
| Source dataset | uspto-grants-2015_02 |
|---|
| ORD ID | ord-dbd8c47c1d3a48f495ece361b8b3e857 |
|---|
| Source note | uspto-grants-2015_02 |
|---|