Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | HCID 13478349 | HCID 13478349 | — |
| Product | HCID 13478351 | HCID 13478351 | — |
Reaction Steps
A mixture of 1.0 g (2.96 mmole) of 5-[4-(4-cyanophenyl)-1-piperazinyl]-6-propyl-2,4-pyrimidinediamine, 15 ml of 95% ethanol and 15 ml of sulfuric acid was heated under reflux at 100° C. for four hours and cooled. The solution was poured into 200 ml of ice water and filtered. The filtrate was kept cool and neutralized with 50% aqueous sodium hydroxide solution to pH 7. The solid was collected and washed with 50 ml of water. Recrystallization from N,N-dimethylformamide and drying in vacuo at 78° C. for 16 hours gave 0.7 g of the product as a white solid, mp 215°-216° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04532240 |
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| Source dataset | uspto-grants-1985_07 |
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| ORD ID | ord-24b676e8d0c14b01abd888ced16dd021 |
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| Source note | uspto-grants-1985_07 |
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