HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluoro-3-(tributylstannyl)pyrazine → HCID 66610755, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluoro-3-(tributylstannyl)pyrazine | HCID 12130662 | — |
| Reactant | 2-Iodo-4-methyl-6-(methylthio)-1,3,5-triazine | HCID 60154716 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 66610755 | HCID 66610755 | 47.3% |
Reaction Conditions
| Temperature | 110 °C |
|---|
Reaction Steps
A mixture of 2-iodo-4-methyl-6-(methylthio)-1,3,5-triazine (100 mg, 0.374 mmol), 2-fluoro-3-(tributylstannyl)pyrazine (145 mg, 0.374 mmol) and tetrakis(triphenylphosphine)palladium(0) (43.3 mg, 0.037 mmol) in toluene (2 mL) was stirred at 110° C. for 18 h. The mixture was cooled down to room temperature. The solvent was removed in vacuo and the residue was purified by silica gel chromatography eluting with 40% EtOAc/hexanes to give 2-(3-fluoropyrazin-2-yl)-4-methyl-6-(methylthio)-1,3,5-triazine (42 mg, 0.177 mmol, 47.3% yield). 1H NMR (300 MHz, CDCl3) δ 8.73 (s, 1H); 8.42 (s, 1H); 2.73 (s, 3H); 2.65 (s, 3H). m/z (ESI, +ve ion) 238.0 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08362241B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-079b3bc4d6864131ae73626037584aac |
| Source note | uspto-grants-2013_01 |