HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725964Generated: October 29, 2026
Potassium Hydroxide → 3-(1-Methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole-5-carboxylic acid
https://huagongshe.com/reaction/725964
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-Methyl-4-piperidone | HCID 74049 | — |
| Reactant | 1H-Indole-5-Carboxylic Acid | HCID 74280 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(1-Methyl-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole-5-carboxylic acid | HCID 19022984 | 71% |
Reaction Steps
To a solution of 5.8 gm (90 mMol) potassium hydroxide in 50 mL methanol were added 4.83 gm (30 mMol) indole 5-carboxylic acid followed by 7.4 mL (60 mMol) 1-methyl-4-piperidone and the resulting solution was heated at reflux for 18 hours. The reaction mixture was then concentrated under reduced pressure and the resulting oil dissolved in 200 mL water. The solution was gradually neutralized by addition of 18 mL 5N hydrochloric acid. The precipitate which formed was isolated by filtration and washed with water to provide 6.09 gm after drying. This solid was dissolved in 100 mL 0.5N sodium hydroxide, filtered and the filtrate treated with 50 mL 1N hydrochloric acid. The solid which formed was filtered and dried under reduced pressure to provide 5.46 gm (71%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05708008 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-bb479d92b6534b93bcd1ba4c857567e4 |
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| Source note | uspto-grants-1998_01 |
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