Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | 1-(4-Chlorophenyl)piperazine | HCID 97478 | — |
| Edukt | HCID 178503521 | HCID 178503521 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | HCID 178517892 | HCID 178517892 | 92,8% |
Reaktionsschritte
20.45 g 1-(4-chloro-phenyl)-piperazine are placed in 5.95 ml (104 mmol) glacial acetic acid and heated to 180° C. 8.01 g 2-methylsulphanyl-6,7-dihydro-thieno[3,2-d]pyrimidin-4-ol are added, the non-stirrable reaction mixture is heated for 2.5 hours to 180° C. After cooling, water is added, the precipitate is suction filtered and dried in the air. The substance is treated with ethanol under ultrasound, suction filtered and dried. 12.95 g of the product are obtained as a powder.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08822474B2 |
|---|
| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-115cf9f5eb3a4b0b9a4d930d5c814dda |
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| Quellennotiz | uspto-grants-2014_09 |
|---|