HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873567Generated: October 30, 2026
Triethylamine → Tert-butyl 4-(4-(1-(pyridazin-3-yl)azetidine-3-carboxamido)phenyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/873567
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,4-Cyclohexadiene | HCID 12343 | — |
| Reactant | Tert-butyl 4-(4-(1-(6-chloropyridazin-3-yl)azetidine-3-carboxamido)phenyl)piperidine-1-carboxylate | HCID 86702042 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | Tert-butyl 4-(4-(1-(pyridazin-3-yl)azetidine-3-carboxamido)phenyl)piperidine-1-carboxylate | HCID 86702044 | — |
Reaction Steps
To a 50 mL round-bottomed flask was added tert-butyl 4-(4-(1-(6-chloropyridazin-3-yl)azetidine-3-carboxamido)phenyl)piperidine-1-carboxylate (550 mg, 1.165 mmol) and Pd/C (93 mg, 0.087 mmol). The flask was flushed with nitrogen for 10 minutes and ethanol (11.7 ml) was added. Triethylamine (0.162 ml, 1.165 mmol) and cyclohexa-1,4-diene (654 mg, 8.16 mmol) were added and the reaction was stirred at 80° C. for 1 hour, cooled and filtered through diatomaceous earth. The filtrate was concentrated in vacuo and the residue was purified by regular phase flash column chromatography to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08975398B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-a82ea6b1561f4fc09794abf23a3a08cc |
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| Source note | uspto-grants-2015_03 |
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