HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532467Generated: October 28, 2026
Sodium Carbonate → 7-(2-Fluoro-4-methanesulfonyl-phenyl)-4-(methylthio)thieno[3,2-d]pyrimidine
https://huagongshe.com/reaction/532467
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 7-Bromo-4-methylsulfanylthieno[3,2-d]pyrimidine | HCID 46928427 | — |
| Reactant | 2-(2-Fluoro-4-(methylsulfonyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 68299298 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 7-(2-Fluoro-4-methanesulfonyl-phenyl)-4-(methylthio)thieno[3,2-d]pyrimidine | HCID 68299336 | — |
Reaction Steps
7-bromo-4-methylsulfanylthieno[3,2-d]pyrimidine (270 mg, 1.03 mmol) was added to 1,4-dioxane (10 mL), and 2-(2-fluoro-4-methanesulfonyl-phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1.5 eq), tetrakis(triphenylphosphine)palladium(0) (71 mg, 0.06 eq), 2N aqueous sodium carbonate (3.1 mL, 3 eq) were sequentially added thereto while stirring. The reaction mixture was degassed with Ar(g), heated to 100° C., and stirred at 100° C. for 4 hours. After completion of the reaction using sodium bicarbonate, the reaction mixture was extracted twice with ethyl acetate. The collected organic layer was dried over anhydrous magnesium sulfate, dried, and concentrated under reduced pressure to obtain a foamy residue. The residue was crystallized in the presence of diethyl ether to obtain the title compound as a yellowish solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853213B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-634055c2529646d3b90768c0faa5f1aa |
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| Source note | uspto-grants-2014_10 |
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