HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910626Generated: November 3, 2026
Hydrochloric Acid → HCID 57584048, compound
https://huagongshe.com/reaction/910626
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 57584192 | HCID 57584192 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57584048 | HCID 57584048 | 88.6% |
Reaction Steps
An aqueous 1 M sodium hydroxide solution (3.0 ml) was added to an ethanol (5 ml)-tetrahydrofuran (5 ml) solution of ethyl 1-{2-[3-(4-{[(2-{[(5-chloropyridin-2-yl)amino]carbonyl}-6-hydroxyphenyl)amino]carbonyl}phenyl)-2-oxopyridin-1(2H)-yl]ethyl}piperidine-4-carboxylate (392 mg), followed by stirring at room temperature for 19 hours. 1 M hydrochloric acid (3.0 ml) and water (50 ml) were added to the reaction mixture, followed by extraction with chloroform-isopropanol. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure to obtain 1-{2-[3-(4-{[(2-{[(5-chloropyridin-2-yl)amino]carbonyl}-6-hydroxyphenyl)amino]carbonyl}phenyl)-2-oxopyridin-1(2H)-yl]ethyl}piperidine-4-carboxylic acid (332 mg) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022208B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-f028d36fc4e74cf8a6bac9e572e27ea2 |
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| Source note | uspto-grants-2011_09 |
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