HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555339Generated: October 29, 2026
L-Serine → 2-acetamido-3-(6-chloro-5-fluoro-1H-indol-3-yl)propanoic acid
https://huagongshe.com/reaction/555339
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | L-Serine | HCID 5951 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 6-Chloro-5-fluoro-1H-indole | HCID 2773648 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-acetamido-3-(6-chloro-5-fluoro-1H-indol-3-yl)propanoic acid | HCID 57948733 | 37% |
Reaction Steps
To a solution of 6-chloro-5-fluoroindole (1.8 g, 10.8 mmol) and Ac2O (10 mL) in AcOH (30 mL) was added L-serine (2.2 g, 20.9 mmol), the mixture was heated to 80° C. After TLC indicated the reaction was complete, the mixture was cooled to 0° C., neutralized to pH 11, and washed with MTBE. The aqueous phase was acidified to pH 2 and extracted with EtOAc. The combined organic layers were washed with water and brine, dried with Na2SO4, filtered, and concentrated. The residue was purified with chromatography (Petroleum ether/EtOAc 1:1) to give 2-acetylamino-3-(6-chloro-5-fluoro-1H-indol-3-yl)-proprionic acid as a light yellow solid (1.2 g, 37% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08053442B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-dd62cebfdb2a4dbe8bf5ac666e609094 |
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| Source note | uspto-grants-2011_11 |
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