HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(3-(Trifluoromethyl)phenyl)-1-piperazineethanol → Ethyl 2-(8-trifluoromethyl-4-quinolinylamino)-5-fluorobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(3-(Trifluoromethyl)phenyl)-1-piperazineethanol | HCID 217994 | — |
| Reactant | Methyl 2-(8-trifluoromethyl-4-quinolinylamino)-5-fluoro-benzoate | HCID 23331699 | — |
| Product | Ethyl 2-(8-trifluoromethyl-4-quinolinylamino)-5-fluorobenzoate | HCID 86737324 | — |
Reaction Steps
Using the procedure of Example 13, methyl 2-(8-trifluoromethyl-4-quinolinylamino)-5-fluoro-benzoate and 2-[-4-(3-trifluoromethylphenyl)-piperazin-1-yl]-ethanol were reacted to obtain 2-[4-3-trifluoromethylphenyl)-piperazin-1-yl]-ethyl 2-(8-trifluoromethyl-4-quinolinylamino)-5-fluorobenzoate. The said product was dissolved in absolute ethanol and an ethanolic solution of hydrogen chloride was added thereto followed by anhydrous ether. The mixture crystallized was vacuum filtered and the product was washed with anhydrous ether and was dried to form the desired hydrochloride salt melting at 230°-240° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04233305 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-6cb0733c43ea4c23ba30073be53b3ff7 |
| Source note | uspto-grants-1980_11 |