HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183285Generated: October 29, 2026
1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acid → HCID 22479820, compound
https://huagongshe.com/reaction/2183285
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acid | HCID 392871 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 22480146 | HCID 22480146 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22479820 | HCID 22479820 | — |
Reaction Steps
A solution of 1-[(tert-butyl)oxycarbonyl]piperidine-4-carboxylic acid (0.317 g, 1.38 mmol) in 12 mL of dichloromethane was added 1-(3-dimethylaminopropyl)-3-ethyl carbodiimide hydrochloride (EDCI) (0.287 g, 1.5 mmol) The solution was stirred at room temperature for 10 min before 3-(3-aminophenyl)-1-perhydro-2H-pyran-2-yl-1H-indazole-5-carbonitrile (0.400 g, 1.25 mmol) was added as a solid. (A small volume of dichloromethane was used to rinse the flask containing the core). The reaction was stirred at room temperature for 12 hours. Even after addition of 0.5 equivalent of carboxylic acid and EDCI, the reaction could not be driven to completion. The crude mixture was partitioned between water and dichloromethane. The crude was isolated as a brown oil. The yield was not calculated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06897231B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-90850d79d7e846d892c2d2b8d0a60d15 |
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| Source note | uspto-grants-2005_05 |
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