Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 59176797 | HCID 59176797 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 20751408 | HCID 20751408 | 64.7% |
Reaction Steps
1 g of (E)-3-(dimethylamino)-1-imidazo[1,2-a]pyridin-3-yl-2-propen-1-one [1-2] was dissolved in 10 mL of n-butanol, then 354 mg of thiourea and 377 mg of sodium methoxide were added, and the mixture was stirred at 85° C. for 2 hours. After cooling back to the room temperature, 868 μL of methyl iodide was added, and stirred at room temperature for 30 minutes. The solvent was distilled off until the volume is halved, the solid thus produced was taken and washed with diethyl ether and with water in the subsequent order, and then dried under reduced pressure to obtain 728 mg of 3-[2-methylthio-4-pyrimidinyl]imidazo[1,2-a]pyridine [1-3] as a grey solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07718801B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-df210168c0fb47bfb2c8f3e98cc495e8 |
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| Source note | uspto-grants-2010_05 |
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