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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79372Generated: October 27, 2026

Triethylamine → 1-((1,5-dimethyl-1H-pyrazol-3-yl)methyl)-4-nitro-3-vinyl-1H-indazole

https://huagongshe.com/reaction/79372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-((1,5-dimethyl-1H-pyrazol-3-yl)methyl)-3-iodo-4-nitro-1H-indazoleHCID 67261255—
ReactantHCID 178506051HCID 178506051—
SolventEthyl AcetateHCID 8857—
SolventTetrahydrofuran 2-propanolHCID 22597222—
Product1-((1,5-dimethyl-1H-pyrazol-3-yl)methyl)-4-nitro-3-vinyl-1H-indazoleHCID 8667221482%

Reaction Conditions

Temperature80 °C

Reaction Steps

To 1-((1,5-dimethyl-1H-pyrazol-3-yl)methyl)-3-iodo-4-nitro-1H-indazole (8.35 g, 21.0 mmol) in THF/IPA (10 mL/30 mL) was added trifluorovinylpotassium borate (5.63 g, 42.0 mmol), 1,1′-bis(diphenylphosphino)ferrocene-palladium(II)dichloride dichloromethane complex (0.858 g, 1.05 mmol) and triethylamine (8.79 mL, 63.1 mmol). The reaction mixture was heated to 80° C. for 16 hours. The mixture was diluted with EtOAc (100 mL), washed with H2O and brine, and concentrated under reduced pressure. The residue was purified by silica gel chromatography (Hexane/EtOAc 5:1) to provide the product (5.12 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841455B2
Source datasetuspto-grants-2014_09
ORD IDord-2393685120a1404b9cc66a0a79ea1865
Source noteuspto-grants-2014_09