HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284811Generated: November 1, 2026
Hydrochloric Acid → 6-((3-Fluorophenyl)amino)-4-(propylamino)nicotinic acid
https://huagongshe.com/reaction/2284811
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl 6-((3-fluorophenyl)amino)-4-(propylamino)nicotinate | HCID 90051842 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 6-((3-Fluorophenyl)amino)-4-(propylamino)nicotinic acid | HCID 90052180 | 57.7% |
Reaction Steps
To a solution of ethyl 6-((3-fluorophenyl)amino)-4-(propylamino)nicotinate (S15, 247 mg) in ethanol (3 mL) and tetrahydrofuran (1.5 mL), 2.0 mol/L aqueous sodium hydroxide (0.78 mL) was added at room temperature, and the mixture was stirred at 50° C. for 1 hour. To the reaction mixture, 2.0 mol/L aqueous sodium hydroxide (0.39 mL) was added at 50° C., and the mixture was stirred at the same temperature for 3 hours. The reaction mixture was cooled to room temperature, and then 1.0 mol/L aqueous hydrochloric acid was added to the reaction mixture until the mixture became acidic. The solid matter was taken by filtration, washed with water, and then dried under reduced pressure to obtain 6-((3-fluorophenyl)amino)-4-(propylamino)nicotinic acid (S16, 130 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145415B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-76c54f410f2448199640d20835ccf9cd |
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| Source note | uspto-grants-2015_09 |
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