HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783514Generated: October 30, 2026
Trifluoroacetic acid → HCID 54308876, compound
https://huagongshe.com/reaction/1783514
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 4-(4-Methylpiperazin-1-yl)aniline | HCID 737253 | — |
| Reactant | HCID 54030904 | HCID 54030904 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 54308876 | HCID 54308876 | 78.5% |
Reaction Steps
Prepared from 400 mg (1.57 mmol) of 1-isopropyl-7-methanesulfinyl-3,4-dihydro-pyrimido[4,5-d]pyrimidin-2(1H)-one, 600 mg (3.14 mmol) of 1-(4-aminophenyl)-4-methylpiperazine and 605 μL (7.85 mmol) of trifluoroacetic acid in 6.4 mL of acetonitrile. The reaction mixture is heated at 85° C. for 48 hours. After the workup, the crude residue is triturated in ethyl acetate/dichloromethane and filtered. The solids are redissolved in dichloromethane, and the solvent is evaporated under a flow of nitrogen while ethyl acetate is added to maintain a volume of 5 mL. The suspension is filtered, and the solids are washed with ethyl acetate/dichloromethane, and dried to give 470 mg (78%) of the title compound:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07501425B1 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-8f8ef3d2b78644d881d49baf3b0135de |
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| Source note | uspto-grants-2009_03 |
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