HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073272Generated: October 26, 2026
Sodium Hydroxide → 3-Amino-6-fluoro-2-(4-chlorophenyl)-4-quinolinecarboxylic acid
https://huagongshe.com/reaction/1073272
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Fluoroisatin | HCID 236566 | — |
| Reactant | 2-Amino-1-(4-chlorophenyl)ethan-1-one hydrochloride | HCID 2798211 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Amino-6-fluoro-2-(4-chlorophenyl)-4-quinolinecarboxylic acid | HCID 15085969 | 95.3% |
Reaction Steps
To a stirred suspension of 7 g of 5-fluoroisatin in 58 ml of water was added a solution of 9.36 g of sodium hydroxide in 33 ml of water. The solution was heated to 85° C. and a solution of 12 g of 2-amino-1-(4-chlorophenyl)ethanone hydrochloride in a mixture of 92 ml of ethanol and 40 ml of tetrahydrofuran and 92 ml of water was added drop-wise over 2 hours. After the addition was complete, the solution was refluxed for an additional 30 minutes and then the ethanol and tetrahydrofuran were removed by distillation. The mixture was cooled to 20° C. and filtered through celite. The filtrate was acidified to pH 4 with acetic acid. The solid was filtered off, washed with water and dried, giving 12.8 g of the desired compound as a yellow solid, mp 241°-243° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04968702 |
|---|
| Source dataset | uspto-grants-1990_11 |
|---|
| ORD ID | ord-5dcee6d70101433ebcaa9e230850c4b0 |
|---|
| Source note | uspto-grants-1990_11 |
|---|