HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282124Generated: October 31, 2026
Potassium Iodide → N-(4-(1-(4-(4-fluorophenyl)piperazin-1-yl)-1-methylethyl)phenylmethyl)acetamide dihydrochloride monohydrate
https://huagongshe.com/reaction/1282124
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Aniline, N,N-bis(2-chloroethyl)-p-fluoro- | HCID 30941 | — |
| Reactant | N-(4-(1-amino-1-methylethyl)phenylmethyl)acetamide | HCID 18423109 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(4-(1-(4-(4-fluorophenyl)piperazin-1-yl)-1-methylethyl)phenylmethyl)acetamide dihydrochloride monohydrate | HCID 18423145 | 22.6% |
Reaction Steps
To a solution of N-(4-(1-amino-1-methylethyl)phenylmethyl)-acetamide (1.55 g) and N,N-di(2-chloroethyl)-4-fluoroaniline (1.5 g) in dimethyl sulfoxide (30 ml) were added potassium carbonate (3.12 g) and potassium iodide (2.50 g) and the mixture was stirred at 80° C. for 24 hr. The reaction mixture was poured into water (300 ml) and extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated and the obtained residue was purified by silica gel chromatography (developing solvent; ethyl acetate:hexane=3:1) and treated with 1M hydrochloric acid-ether in ethanol to give the title compound (0.33 g) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06455528B1 |
|---|
| Source dataset | uspto-grants-2002_09 |
|---|
| ORD ID | ord-e5489caa0e9b47868fbcc60aa2f95bca |
|---|
| Source note | uspto-grants-2002_09 |
|---|