HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426277Generated: November 2, 2026
Toluene → 2-Chloro-5-(2-ethoxy-vinyl)-pyrimidin-4-ylamine
https://huagongshe.com/reaction/2426277
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | 4-Amino-5-bromo-2-chloropyrimidine | HCID 2763293 | — |
| Reactant | (Z)-1-Ethoxy-2-(tributylstannyl)ethene | HCID 2763294 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Chloro-5-(2-ethoxy-vinyl)-pyrimidin-4-ylamine | HCID 57348973 | 46% |
Reaction Steps
A 500 mL round bottomed flask is charged with 5-bromo-2-chloropyrimidin-4-ylamine (1) (10 g, 48 mmol), tetrakis(triphenylphosphine)palladium(0) (2.8g, 2.5 mmol), and toluene (200 mL). Tributyl-(2-ethoxyvinyl)-stannane (22 g, 60 mmol) is added and the reaction heated to 110° C. with stirring for approximately 15 hours. After cooling to room temperature, the solution is diluted with 100 mL ethyl acetate and washed with water and brine. The organic extract is dried over Na2SO4, filtered, and concentrated under reduced pressure. Purification by column chromatography (SiO2, Hexane:Ethyl acetate/5:1) provides 2 (4.4 g, 46%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07968557B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-fd9622c534054b589b3de758a0ec4964 |
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| Source note | uspto-grants-2011_06 |
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