Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109953Generated: October 26, 2026

Cesium carbonate → 3-[(3-tert-butyl-1-methyl-1H-pyrazol-5-yl)amino]pyridine-2-carbonitrile

https://huagongshe.com/reaction/2109953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantBinap, (A+-)-HCID 634876—
Reactant3-Bromopyridine-2-carbonitrileHCID 817694—
Reactant3-tert-Butyl-1-methyl-1H-pyrazol-5-amineHCID 2735287—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product3-[(3-tert-butyl-1-methyl-1H-pyrazol-5-yl)amino]pyridine-2-carbonitrileHCID 5763581558%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 3-bromopyridine-2-carbonitrile (150 mg, 0.98 mmol), 3-tert-butyl-1-methyl-1H-pyrazol-5-amine (179 mg, 0.98 mmol), cesium carbonate (638 mg, 1.96 mmol), BINAP (98 mg, 0.16 mmol) and Pd2(dba)3 (90 mg, 0.10 mmol) was taken in anhydrous toluene (2 mL) and heated to 80° C. for 24 h under nitrogen atmosphere. The reaction mixture was cooled to rt, diluted with ethyl acetate, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography using EtOAc/Hex (1:9 to 1:4, v/v) as the eluent. The product was obtained as a yellow oil (145 mg, 58%). ES-MS m/z 256.1 (MH+); HPLC RT (min) 2.37.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517878B2
Source datasetuspto-grants-2009_04
ORD IDord-db151f4822a9469ca071079bb5e0e5e3
Source noteuspto-grants-2009_04