Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504861Generated: November 1, 2026

Cesium carbonate → Tert-butyl [3-({6-cyano-5-[(4,6-dimethylpyridin-2-yl)amino]pyridin-3-yl}amino)-1-(methylamino)-1-oxopropan-2-yl]carbamate

https://huagongshe.com/reaction/1504861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Reactant5-Bromo-3-[(4,6-dimethylpyridin-2-yl)amino]pyridine-2-carbonitrileHCID 86731650—
ReactantTert-butyl 3-amino-1-(methylamino)-1-oxopropan-2-ylcarbamateHCID 86731730—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
ProductTert-butyl [3-({6-cyano-5-[(4,6-dimethylpyridin-2-yl)amino]pyridin-3-yl}amino)-1-(methylamino)-1-oxopropan-2-yl]carbamateHCID 86731729—

Reaction Conditions

Temperature100 °C

Reaction Steps

Dioxane (1.65 ml) was added to a nitrogen purged flask containing 5-bromo-3-[(4,6-dimethylpyridin-2-yl)amino]pyridine-2-carbonitrile (PrepEx 1.4) (100 mg, 0.330 mmol), tert-butyl 3-amino-1-(methylamino)-1-oxopropan-2-ylcarbamate (72 mg, 0.33 mmol), Xantphos (19 mg, 0.033 mmol), Pd2(dba)3 (24 mg, 0.026 mmol) and cesium carbonate (215 mg, 0.660 mmol). Nitrogen was bubbled through the reaction mixture for 5 minutes. The reaction vessel was then sealed and heated at 100° C. for 2 hours. The reaction mixture was cooled to room temperature, filtered through CELITE, and the filter cake was washed with ethyl acetate (10 mL). The filtrate was concentrated under reduced pressure. The residue was purified by silica gel chromatography (0-5% methanol/ethyl acetate, linear gradient) to afford tert-butyl [3-({6-cyano-5-[(4,6-dimethylpyridin-2-yl)amino]pyridin-3-yl}amino)-1-(methylamino)-1-oxopropan-2-yl]carbamate. MS ESI calc'd. for C22H30N7O3 [M+H]+ 440. found 440.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216173B2
Source datasetuspto-grants-2015_12
ORD IDord-f735f951f1944937a0fae4e1847b836a
Source noteuspto-grants-2015_12