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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589914Generated: October 31, 2026

Dimethylformamide → 4-((3-aminophenyl)ethynyl)-1H-indazol-3-amine

https://huagongshe.com/reaction/589914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriphenylphosphineHCID 11776—
ReactantBenzenamine, 3-ethynyl-HCID 104682—
Reactant4-iodo-1H-indazol-3-amineHCID 4057787—
CatalystCopper iodideHCID 83717—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTriethylamineHCID 8471—
Product4-((3-aminophenyl)ethynyl)-1H-indazol-3-amineHCID 118638425—

Reaction Conditions

Temperature60 °C

Reaction Steps

To 8 ml of DMF was added 4-iodo-1H-indazol-3-amine (690 mg, 2.65 mmol) and 3-ethynylaniline (480 mg, 1.5 eq., 4.1 mmol). Following that, Bis(triphenylphosphine) palladium(II) dichloride (180 mg, 0.25 mmol, 10 mol %), Copper Iodide (100 mg, 0.52 mmol, 20 mol %), Triphenylphosphine (18 mg, 0.07 mmol, 3 mol %) and 8 ml of triethylamine was added. Nitrogen was bubbled through the reaction mixture for 15 minutes. The reaction was then set with a reflux condenser, set under nitrogen atmosphere, and heated at 60° C. for 2 hours. After that, the reaction was cooled to room temperature and 40 ml of ethyl acetate was added. The organic layer was extracted with aqueous sodium bicarbonate (3×40 ml), brine (3×40 ml), dried using anhydrous sodium sulfate, loaded onto silica and columned to give 4-((3-aminophenyl)ethynyl)-1H-indazol-3-amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233968B1
Source datasetuspto-grants-2016_01
ORD IDord-e1fda866a7f34f3db769165eb6f574ac
Source noteuspto-grants-2016_01