Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | HCID 178477353 | HCID 178477353 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178517891 | HCID 178517891 | 91.2% |
Reaction Steps
6.4 g (39 mmol) of N-phenylpiperazine (III) is placed in 2.2 mL of glacial acetic acid, heated to 125° C., then 3.2 g (15 mmol) of 2-ethylsulfanyl-6,7-dihydrothieno[3,2-d]pyrimidin-4-ol (II) is added, and the mixture is heated to 175° C. After 1.5 hours, the resulting solid is stirred with water, suction filtered, washed with ethanol, and dried. 4.3 g product (91%) is obtained as a powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07511045B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-feb837468fb14674a93043c3a885c4ee |
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| Source note | uspto-grants-2009_03 |
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