Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | HCID 6919148 | HCID 6919148 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 15434275 | HCID 15434275 | 43.9% |
Reaction Steps
0.56 g (1.9 mmol) of 2-(4-benzoyl-1-piperazinyl)-4-methoxypyrimidine are dissolved in 25 mL of dry toluene, and 0.46 g (1.14 mmol) of Lawesson's reagent (2,4-bis(4-methoxyphenyl)-1,32,4-dithiadiphosphaethano-2,4-disulphide) added. The mixture is heated to 80-90° C. for 16 hours. Ethyl ether is added, basic water is used to wash the residue and the organic extract is dried with NaSO4 and the solvent evaporated off under reduced pressure. The resulting crude residue is crystallised with ethyl ether-petroleum ether to give 160 mg (0.5 mmol) of 2-(4-thiobenzoyl-1-piperazinyl)-4-methoxypyrimidine. m.p.=125-129° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06372746B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-7341554352ab4d4796276e4a14f85c78 |
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| Source note | uspto-grants-2002_04 |
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