HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357955Generated: October 30, 2026
Acetonitrile → 1-(t-Butoxycarbonyl)-4-(3-benzyl-1-ethyl-(1H)-pyrazol-5-yl)piperidine
https://huagongshe.com/reaction/1357955
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Ethylhydrazine | HCID 29062 | — |
| Reactant | Tert-butyl 4-(3-oxo-4-phenylbutanoyl)piperidine-1-carboxylate | HCID 18187492 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(t-Butoxycarbonyl)-4-(3-benzyl-1-ethyl-(1H)-pyrazol-5-yl)piperidine | HCID 18187719 | — |
Reaction Steps
A 100 L cylindrical flask with a bottom valve was equipped with a mechanical stirrer, internal heating coil, 5 L dropping funnel, and thermocouple was charged with the acetonitrile (39 L) and 1-(1-(t-butoxycarbonyl)piperidin-4-yl)-4-phenylbutane-1,3-dione 4 (3.00 Kg, 8.68 mol). To the resulting clear light yellow solution was added water (18.6 l). The mixture was warmed to 19° C. and the mixture became clear. An ethyl hydrazine solution (35% in water, 1.66 Kg, 1.71 L, 9.55 mol) was added via a dropping funnel over 100 min. The batch temperature after the addition was 20° C. The reaction solution was aged for 1 h at 20° C. then checked for completion by HPLC. If any 4 remained, additional ethyl hydrazine was added to complete the reaction. At the end of reaction the ratio of products 5:6:7 is 83.6:14.3:2.1 with complete consumption of 4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06593346B2 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-1d5b7493a76d47c5b144f8a61bb48747 |
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| Source note | uspto-grants-2003_07 |
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