HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260925Generated: November 1, 2026
1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acid → HCID 86631298, compound
https://huagongshe.com/reaction/1260925
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acid | HCID 392871 | — |
| Reactant | HCID 86631295 | HCID 86631295 | — |
| Catalyst | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Catalyst | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86631298 | HCID 86631298 | 99.7% |
Reaction Steps
A mixture of N-[(3R*,4R*)-3-(3,4-dichlorophenyl)piperidin-4-yl]-N-methyl-3,5-bis(trifluoromethyl)benzamide monohydrochloride (0.90 g) obtained in Example 2, N-Boc-isonipecotic acid (1.52 g), WSC.HCl (0.82 mg) and HOBt (0.65 mg) was stirred at room temperature for 2 hr. The reaction mixture was poured into water, and the resultant product was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate solution and brine and dried, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent gradient; 50→100% ethyl acetate/hexane, then 0→10% methanol/ethyl acetate) to give the title compound (1.19 g, 59%) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08470816B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-21f40dc9d9474169a0f23f20fd380248 |
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| Source note | uspto-grants-2013_06 |
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