HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 9916355, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 1-Biphenyl-4-yl-piperazine | HCID 2735513 | — |
| Reactant | 9-(4-Bromobutyl)-N-(2,2,2-trifluoroethyl)-9H-fluorene-9-carboxamide | HCID 10526437 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 9916355 | HCID 9916355 | — |
Reaction Steps
A solution of 0.4 g (1.678 mmol) of 1-biphenyl-4-yl-piperazine, 0.682 g (1.6 mmol) of 9-(4-bromo-butyl)-9H-fluorene-9-carboxylic acid-(2,2,2-trifluoroethyl)-amide and 0.223 ml (1.6 mmol) of triethylaminein 20 ml acetonitrile is stirred for 14 hours at 60° C. and then diluted with water. It is extracted with ethyl acetate and the organic phase is dried over sodium sulphate. Purification is by column chromatography on silica gel (eluant: dichloromethane/ethanol=40:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06818644B1 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-7ec0247150ee4a61a1ac5e73fd82fcde |
| Source note | uspto-grants-2004_11 |