HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222236Generated: October 30, 2026
Benzoylhydrazine → HCID 67109702, compound
https://huagongshe.com/reaction/222236
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoylhydrazine | HCID 11955 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1-[(Pyridin-3-yloxy)carbonyl]piperidine-4-carboxylic acid | HCID 57421842 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67109702 | HCID 67109702 | 55.3% |
Reaction Steps
To a mixture of 1-[(pyridin-3 yloxy)carbonyl]piperidine-4-carboxylic acid (1.5 g) and DCM (15 mL) were added 1-hydroxybenzotriazole (HOBt) (0.85 g), benzohydrazine (0.86 g), and 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (WSC) hydrochloride (1.21 g), followed by stirring at room temperature for about 15 hours. To the reaction liquid were added chloroform and water, and the organic phase was separated. The organic phase was washed with water and saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (chloroform/methanol=100/0 to 90/10). To the purified product were added diisopropyl ether and methanol, and the resulting solid was collected by filtration and dried under reduced pressure to obtain pyridin-3-yl 4-[(2-benzoylhydrazino)carbonyl]piperidine-1-carboxylic acid (1.22 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207199B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-30924eb689ba4c4084f2e05530f6d999 |
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| Source note | uspto-grants-2012_06 |
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