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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064544Generated: October 26, 2026

2,4-Pentanedione, 3-benzyl- → 4-(4-Benzyl-3,5-dimethyl-pyrazol-1-yl)-6-pyridin-2-yl-[1,3,5]triazin-2-ylamine

https://huagongshe.com/reaction/1064544

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Pentanedione, 3-benzyl-HCID 97757—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant4-Hydrazinyl-6-(pyridin-2-yl)-1,3,5-triazin-2-amineHCID 608952—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product4-(4-Benzyl-3,5-dimethyl-pyrazol-1-yl)-6-pyridin-2-yl-[1,3,5]triazin-2-ylamineHCID 22174870—

Reaction Conditions

Temperature75 °C

Reaction Steps

A suspension of 4-hydrazino-6-pyridin-2-yl-[1,3,5]triazin-2-ylamine (5.25 g, 25.6 mmol), 3-benzylpentane-2,4-dione (5.0 g, 28.4 mmol), and p-toluenesulfonic acid monohydrate (0.475 g, 2.50 mmol) in dimethylsulfoxide (50 mL) was heated to 75° C. for 20 hours. The reaction mixture was allowed to cool to room temperature, and the suspension was dissolved in methylene chloride (700 mL). The solution was washed three times with water, once with brine, dried (magnesium sulfate), and concentrated to afford a moist solid. The crude product was suspended in ethyl acetate (50 mL), heated to reflux, allowed to cool to room temperature, and filtered (repeated three times). The final product was obtained as a white solid containing 3% dimethylsulfoxide by weight: 8.63 g (90%). 1H NMR (CDCl3) δ 8.84-8.53 (m, 1H), 8.48 (d, J=7.9 Hz, 1H), 7.86-7.91 (m, 1H), 7.46-7.50 (m, 1H), 7.13-7.30 (m, 5H), 6.61 (br s, 1H), 6.40 (br s, 1H), 3.83 (s, 2H), 2.79 (s, 3H), 2.24 (s, 3H) ppm. MS (ESI) m/z 358 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969728B2
Source datasetuspto-grants-2005_11
ORD IDord-f87f65eaae3444d8a6415f0346c1362b
Source noteuspto-grants-2005_11