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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875452Generated: November 1, 2026

Cesium carbonate → 6-(3-(2-fluorobenzyl)-1H-indazol-1-yl)-1,3,5-triazine-2,4-diamine

https://huagongshe.com/reaction/1875452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant1,3,5-Triazine-2,4-diamine, 6-chloro-HCID 18831—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
ReactantHCID 178505618HCID 178505618—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product6-(3-(2-fluorobenzyl)-1H-indazol-1-yl)-1,3,5-triazine-2,4-diamineHCID 24794477—

Reaction Conditions

Temperature90 °C

Reaction Steps

Under argon, 130 mg (0.58 mmol) of 3-(2-fluorobenzyl)-1H-indazole from example 5A, 84 mg (0.58 mmol) of 6-chloro-1,3,5-triazine-2,4-diamine, 11 mg (0.011 mmol) of tris(dibenzylidene-acetone)dipalladium, 16 mg (0.034 mmol) of dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (XPHOS) and 262 mg (0.80 mmol) of cesium carbonate are introduced into 4 ml of degassed toluene and heated at 90° C. for 20 h. The mixture is then diluted with ethyl acetate and methanol, filtered and concentrated in vacuo. The residue is purified by preparative HPLC to result in 36 mg (19% of theory) of the title compound. In addition, 65 mg of the starting compound are recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309551B2
Source datasetuspto-grants-2012_11
ORD IDord-31846d97e9444bd99fcad11442b94617
Source noteuspto-grants-2012_11