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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41373Generated: October 28, 2026

Hydrazine → 4-[[5-Amino4-[(2,4,6-trimethylphenyl)amino]-2-pyrimidinyl]amino]benzonitrile

https://huagongshe.com/reaction/41373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
Reactant4-[[4-[(2,4,6-Trimethylphenyl)amino]-5-nitro-2-pyrimidinyl]amino]benzonitrileHCID 22170095—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-[[5-Amino4-[(2,4,6-trimethylphenyl)amino]-2-pyrimidinyl]amino]benzonitrileHCID 2217008770%

Reaction Steps

4-[[4-[(2,4,6-trimethylphenyl)amino]-5-nitro-2-pyrimidinyl]amino]benzonitrile (0.001 mol), Pd/C 10% (0.025 g), ethanol (20 ml), and hydrazine (0.030 mol) were combined to form a slurry and stirred at room temperature for 16 hours. The solvent was removed by rotary evaporation. The residue was taken up in tetrahydrofuran (20 ml) and methanol (1 ml). A second portion of hydrazine (0.5 g) was added, and the reaction was stirred for 16 hours at room temperature. A third portion of hydrazine (0.5 ml) was added and the reaction was stirred for an additional 16 hours at room temperature. The sample was concentrated by rotary evaporation onto silica gel (1 g) and purified by flash chromatography (eluent: 0.5, 1, 2% 10% (NH4OH in CH3OH) in CH2Cl2). The desired fractions were purified by preparatory HPLC to yield 0.24 g of 4-[[5-amino-4-[(2,4,6-trimethylphenyl)amino]-2-pyrimidinyl]amino]benzonitrile (70%); mp. 224-225° C. (comp. 51).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530655B2
Source datasetuspto-grants-2013_09
ORD IDord-c842046da6e3450690c4464adfb7ff7d
Source noteuspto-grants-2013_09