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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Isopropylhydrazine hydrochlorideHCID 85573—
ReactantBenzyl (3-Oxopropyl)carbamateHCID 10398106—
ReactantHCID 67047481HCID 67047481—
SolventIsopropanolHCID 3776—
Product{2-[4-[1,3]Dioxolan-2-ylmethyl-5-(4-fluoro-phenyl)-1-isopropyl-1H-pyrazol-3-yl]-ethyl}-carbamic acid benzyl esterHCID 54754013—

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915404B2
Source datasetuspto-grants-2011_03
ORD IDord-b69b21dd81c34ab1861ce9f0a5fd3e71
Source noteuspto-grants-2011_03