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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401163Generated: October 25, 2026

Water → 5-bromo-6-chloro-2-(1H-pyrazol-1-yl)pyrimidin-4-amine

https://huagongshe.com/reaction/2401163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyrazoleHCID 1048—
ReactantCesium carbonateHCID 10796—
Reactant5-Bromo-6-chloro-2-methanesulfinylpyrimidin-4-amineHCID 86677016—
SolventDimethylformamideHCID 6228—
Product5-bromo-6-chloro-2-(1H-pyrazol-1-yl)pyrimidin-4-amineHCID 8667701765%

Reaction Steps

1 g (3.7 mmol) of 5-bromo-6-chloro-2-(methylsulfinyl)pyrimidine-4-amine (intermediate 2) was suspended in 10 ml of DMF. To this suspension were added 0.33 g (4.8 mmol) de pyrazole and 0.8 g of cesium carbonate. The reaction mixture was turned immediately light yellow color and allowed to stir at room temperature for about 1 to 2 hours. After nearly complete conversion to the corresponding monosubstituted derivative as was indicated by TLC the solution was poured onto 100 ml of cool water. The formed precipitated was filtered, washed with water and dried to afford 0.66 g (65%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796284B2
Source datasetuspto-grants-2014_08
ORD IDord-be51a176488d42638229ef21fd1ee146
Source noteuspto-grants-2014_08