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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2386591Generated: October 27, 2026

Diisopropylethylamine → c-Met inhibitor 1

https://huagongshe.com/reaction/2386591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant5-iodo-2-methyl-2H-indazoleHCID 40154007—
ReactantHCID 178480034HCID 178480034—
CatalystTris(dibenzylideneacetone) dipalladiumHCID 9832798—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Productc-Met inhibitor 1HCID 5665091552.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 6-(1-methyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[4,3-b]pyridazine-3-thiol (2.3 g, 10.0 mmol) in DMF (20 mL) is added 5-iodo-2-methyl-2H-indazole (2.6 g, 10.0 mmol), tris(dibenzylideneacetone) dipalladium(0) (460 mg; 502.7 μmol), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (580 mg, 1.0 mmol), diisopropylethylamine (4 mL, 22.9 mmol). The mixture is purged with N2 and stirred at 100° C. for 18 h. DMF is removed under vacuum, and the residue is purified by flash column chromatography (Combi-Flash, silica gel) eluting with DCM/methanol (20:1) to give a crude product. The crude product is suspended in 20 mL of DCM to give slurry, and the pure product is collected by filtration to afford the title compound (1.9 g, 52.5%) as a yellow solid. MS (m/z): 363.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268836B2
Source datasetuspto-grants-2012_09
ORD IDord-ea678d841d664d46882c6b3762643dbb
Source noteuspto-grants-2012_09