HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807720Generated: October 26, 2026
Trifluoroacetic acid → (4-Amino-3-fluorophenyl)(piperazin-1-yl)methanone
https://huagongshe.com/reaction/1807720
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Tert-butyl 4-(4-amino-3-fluorobenzoyl)piperazine-1-carboxylate | HCID 58055815 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (4-Amino-3-fluorophenyl)(piperazin-1-yl)methanone | HCID 63187976 | — |
Reaction Steps
tert-Butyl 4-(4-amino-3-fluorobenzoyl)piperazine-1-carboxylate (0.649 mmol, 210 mg) was stirred with dichloromethane (˜2 mL) and trifluoroacetic acid (˜0.5 mL) overnight. The mixture was purified by SCX chromatography to give the intermediate (4-amino-3-fluorophenyl)(piperazin-1-yl)methanone. 2-(4-(Bromomethyl)phenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol (0.649 mmol, 219 mg), potassium carbonate (0.649 mmol, 90 mg) and acetonitrile (5 mL) were added to the intermediate (4-amino-3-fluorophenyl)(piperazin-1-yl)methanone and the mixture was stirred for 6 hours. The reaction mixture was concentrated under reduced pressure. The residue obtained was stirred in dichloromethane, filtered and the filtrate was purified by silica chromatography (eluting with dichloromethane increasing to ethyl acetate) to afford the title compound (46 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08357679B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-1a4b70f9c88d4e0d85cd87c1c02093c0 |
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| Source note | uspto-grants-2013_01 |
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