HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889384Generated: November 3, 2026
Potassium Carbonate → 4'-[(6-cyclopropyl-2,4-dioxo-3,4-dihydrothieno[2,3-d]pyrimidin-1(2H)-yl)methyl]-3',5'-difluorobiphenyl-2-carbonitrile
https://huagongshe.com/reaction/1889384
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4'-(Bromomethyl)-3',5'-difluorobiphenyl-2-carbonitrile | HCID 57460541 | — |
| Reactant | 6-cyclopropyl-3-(2,4-dimethoxybenzyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione | HCID 59351745 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4'-[(6-cyclopropyl-2,4-dioxo-3,4-dihydrothieno[2,3-d]pyrimidin-1(2H)-yl)methyl]-3',5'-difluorobiphenyl-2-carbonitrile | HCID 59351597 | 94% |
Reaction Steps
A mixture of 6-cyclopropyl-3-(2,4-dimethoxybenzyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione (0.37 g), 4′-(bromomethyl)-3′,5′-difluorobiphenyl-2-carbonitrile (0.38 g), potassium carbonate (0.29 g) and acetonitrile (30 mL) was stirred at 50° C. for 2 hr. Insoluble material was filtered off, and the solvent was evaporated under reduced pressure. The obtained residue was dissolved in trifluoroacetic acid (10 mL), and the mixture was stirred at 50° C. for 2 hr. To the reaction mixture was added toluene (10 mL), and the mixture was concentrated under reduced pressure. To the obtained residue was added ethyl acetate (10 mL), and the mixture was concentrated under reduced pressure. The precipitated solid was collected by filtration to give the title compound as a colorless solid (0.42 g, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08501750B2 |
|---|
| Source dataset | uspto-grants-2013_08 |
|---|
| ORD ID | ord-61ebecf4c5564f1cbedb0971d5715a58 |
|---|
| Source note | uspto-grants-2013_08 |
|---|