HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 838948Generated: October 31, 2026
Sodium hydride → 2-[4-(4-Chlorophenyl)-1-piperazinyl]-ethyl 3-(8-trifluoromethyl 4-quinolylamino)-2-thiophene-carboxylate
https://huagongshe.com/reaction/838948
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-[4-(4-Chlorophenyl)piperazin-1-yl]ethanol | HCID 258211 | — |
| Reactant | Methyl 3-(8-trifluoromethyl-4-quinolylamino)-2-thiophene-carboxylate | HCID 15916787 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-[4-(4-Chlorophenyl)-1-piperazinyl]-ethyl 3-(8-trifluoromethyl 4-quinolylamino)-2-thiophene-carboxylate | HCID 20325466 | 76.7% |
Reaction Steps
A mixture of 7.04 g of methyl 3-(8-trifluoromethyl-4-quinolylamino)-2-thiophene-carboxylate, 5.5 g of 4-(4-chlorophenyl)-1-piperazine ethanol and 50 ml of anhydrous toluene was refluxed for an hour while passing condensed toluene through a column filled with siliporite and after cooling the mixture to 60° C, 150 ml of sodium hydride were added. The mixture was refluxed with stirring for 16 hours and the toluene was distilled. The residue was extracted with methylene chloride, was washed and dried. The product was crystallized from 95% ethanol, iced and vacuum filtered. The precipitate was washed with ethanol and dried to obtain 8.6 g of 2-[4-(4-chlorophenyl)-1-piperazinyl]-ethyl 3-(8-trifluoromethyl 4-quinolylamino)-2-thiophene-carboxylate melting at 155° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04093724 |
|---|
| Source dataset | uspto-grants-1978_06 |
|---|
| ORD ID | ord-cdb6d4f942434e97a4b5e05c05f13702 |
|---|
| Source note | uspto-grants-1978_06 |
|---|