HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200929Generated: October 30, 2026
HCID 367509, compound → HCID 58032590, compound
https://huagongshe.com/reaction/2200929
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 367509 | HCID 367509 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 7H-purin-8-amine | HCID 12178861 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58032590 | HCID 58032590 | — |
Reaction Steps
Under an atmosphere of argon, 7H-purine-8-amine (300 mg, 2.2 mmol) and ethyl 2-(4-cyanobenzylidene)-3-oxobutanoate (702 mg, 2.9 mmol, 1.3 eq.) were dissolved in DMF (5 ml), and solid sodium bicarbonate (932 mg, 11.1 mmol, 5 eq.) was added. The mixture was stirred at 55° C. for 12 h. The mixture was then filtered, and the DMF from the filtrate was distilled off under reduced pressure. The residue was purified by preparative HPLC (Gromsil C18 column, 30×250 mm; mobile phase: acetonitrile-water-0.1% TFA 10:90→90:10). After lyophilization of the appropriate fractions, the title compound was obtained as a solid (430 mg, 54% of theory). The isomeric compound (rac)-ethyl 9-(4-cyanophenyl)-7-methyl-6,9-dihydropyrimido[1,2-e]purine-8-carboxylate (see Example 23A) was obtained as a byproduct.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09359362B2 |
|---|
| Source dataset | uspto-grants-2016_06 |
|---|
| ORD ID | ord-9b5dbd53ebc247f4914a58b98d07c58d |
|---|
| Source note | uspto-grants-2016_06 |
|---|