HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250032Generated: November 2, 2026
Acetic Acid → 5-Chloro-1-(4-fluorophenyl)-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole
https://huagongshe.com/reaction/1250032
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 5-Chloro-1-(4-fluorophenyl)-1H-indole | HCID 10236188 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 5-Chloro-1-(4-fluorophenyl)-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole | HCID 9883838 | — |
Reaction Steps
5-chloro-1-(4-fluorophenyl)indole (6.70 kg) and 4-piperidone-mono-hydrate,hydrochloride (8.38 kg) were transferred to a 200 L reactor under N2 cover. Acetic acid (67 L) was added and the reaction mixture was heated to 60° C. Concentrated HCl (37%, 33.5 L) was added during ½ hour and then the mixture was heated to the reflux temperature (85° C.) and refluxed for 1 hour (final temperature 95° C.). After cooling to 30° C., 33.5 L acetone was added followed by further cooling to 25° C. Filtration, wash (acetone 20 L) and drying in vacuum at 60° C. gave the title product as a white powder, yield 8.94 kg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06335463B1 |
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| Source dataset | uspto-grants-2002_01 |
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| ORD ID | ord-de443f8748cc4b6b8bd50426c69e2f7b |
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| Source note | uspto-grants-2002_01 |
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