HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494911Generated: October 31, 2026
Methanol → 1-(1-benzyloxycarbonylpiperidin-4-yl)-1H-indole-6-carboxylic acid
https://huagongshe.com/reaction/494911
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | methyl 1-(1-benzyloxycarbonylpiperidin-4-yl)-1H-indole-6-carboxylate | HCID 57682829 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(1-benzyloxycarbonylpiperidin-4-yl)-1H-indole-6-carboxylic acid | HCID 57682906 | 87.1% |
Reaction Steps
90.0 g of methyl 1-(1-benzyloxycarbonylpiperidin-4-yl)-1H-indole-6-carboxylate was dissolved in a mixed solution consisting of 760 ml of methanol and 200 ml of tetrahydrofuran. Thereafter, 92 ml of a 5 N sodium hydroxide aqueous solution was added to the reaction solution, and the mixture was then heated to a temperature between 60° C. and 70° C. After completion of the reaction, the reaction solution was cooled, and 65.0 g of ammonium chloride was added thereto, followed by concentration under a reduced pressure. A 5% KHSO4 aqueous solution was added to the residue, so as to adjust pH to be 5 to 6, followed by extraction with ethyl acetate. The organic layer was washed with water and a saturated sodium chloride solution, and then dried over anhydrous magnesium sulfate. After removing the drying agent by filtration, the organic layer was concentrated under a reduced pressure. Thereafter, the residue was solidified, and then collected from a mixed solvent consisting of hexane and t-butylmethyl ether by filtration, so as to obtain 75.6 g of the subject compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07538123B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-2d6025b98000440eb5e73734c5cfb996 |
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| Source note | uspto-grants-2009_05 |
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