HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415140Generated: October 27, 2026
Water → 9-[4-(4-phenyl-piperazin-1-yl)-butyl)-9H-fluorene-9-carboxylic acid-(2,2,2-trifluoro-ethyl)-amide
https://huagongshe.com/reaction/2415140
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 9-(4-Bromobutyl)-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide | HCID 10526437 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 9-[4-(4-phenyl-piperazin-1-yl)-butyl)-9H-fluorene-9-carboxylic acid-(2,2,2-trifluoro-ethyl)-amide | HCID 15475487 | — |
Reaction Steps
A suspension of 0.4 g (0.93 mmol) of 9-(4-bromo-butyl)-9H-fluorene-9-carboxylic acid-(2,2,2-trifluoroethyl)-amide, 0.153 ml (1 mmol) of 1-phenylpiperazine, 0.8 g of potassium carbonate and 1 ml water in 30 ml dimethylformamide is stirred for 10 hours at 80° C. The reaction mixture is then poured onto water, extracted with ethyl acetate and the organic phase is dried over sodium sulphate. Purification is by column chromatography on silica gel (eluant: dichloromethane/methanol=15:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06818644B1 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-b269b73281cf43b2b934b1301f00ebd6 |
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| Source note | uspto-grants-2004_11 |
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