HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606623Generated: October 31, 2026
Triethylamine → {2-[4-[1,3]Dioxolan-2-ylmethyl-5-(4-fluoro-phenyl)-1-isopropyl-1H-pyrazol-3-yl]-ethyl}-carbamic acid benzyl ester
https://huagongshe.com/reaction/606623
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Isopropylhydrazine hydrochloride | HCID 85573 | — |
| Reactant | Benzyl (3-Oxopropyl)carbamate | HCID 10398106 | — |
| Reactant | HCID 67047481 | HCID 67047481 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | {2-[4-[1,3]Dioxolan-2-ylmethyl-5-(4-fluoro-phenyl)-1-isopropyl-1H-pyrazol-3-yl]-ethyl}-carbamic acid benzyl ester | HCID 54754013 | — |
Reaction Steps
A solution of isopropylhydrazine hydrochloride (1.06 g, 9.6 mmol), (3-oxo-propyl)-carbamic acid benzyl ester (2.0 g, 9.6 mmol), and Et3N (3.9 g, 38.4 mmol) in isopropanol (30 mL) was heated to reflux. After 3 h, the solution was treated with 2-[3-(4-fluoro-phenyl)-2-nitro-allyl]-[1,3]dioxolane (2.2 g, 8.7 mmol) and stirred at 60° C. for 18 h. The mixture was cooled to rt and concentrated. The residue was partitioned between EtOAc and water. The organic layer was separated, dried (MgSO4), and concentrated. Purification by FCC gave the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915404B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-b69b21dd81c34ab1861ce9f0a5fd3e71 |
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| Source note | uspto-grants-2011_03 |
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