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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220084Generated: October 26, 2026

Ethanol → 5-Methyl-2-(6-methylsulfanyl-pyrimidin-4-yl)-2H-pyrazol-3-ylamine

https://huagongshe.com/reaction/220084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantButanenitrile, 3-imino-HCID 70698—
Reactant4-Hydrazinyl-6-(methylthio)pyrimidineHCID 13519855—
SolventEthyl AcetateHCID 8857—
Product5-Methyl-2-(6-methylsulfanyl-pyrimidin-4-yl)-2H-pyrazol-3-ylamineHCID 59173368—

Reaction Conditions

Temperature85 °C

Reaction Steps

The mixture of (6-Methylsulfanyl-pyrimidin-4-yl)-hydrazine (1.0 g, 6.4 mmol), 3-Imino-butyronitrile (1.1 g, 12.8 mmol), and ethanol (30 mL) is heated to 85° C. for overnight. The reaction mixture is then cooled to room temperature, condensed, and treated with 75 mL ethyl acetate. The reaction mixture is partitioned between ethyl acetate and aqueous layer. The organic layer is dried over Na2SO4 and concentrated. The crude product is purified by ISCO chromatography eluting with ethyl acetate in hexanes from 10% to 80% to afford 5-Methyl-2-(6-methylsulfanyl-pyrimidin-4-yl)-2H-pyrazol-3-ylamine: 1H NMR 400 MHz (d6-DMSO) δ 8.72 (s, 1H), 7.53 (s, 1H), 6.90 (s, 1H), 5.26 (s, 1H), 2.57 (s, 3H), 2.08 (s, 3H); MS m/z 222.07 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202876B2
Source datasetuspto-grants-2012_06
ORD IDord-e8f9c9326c874781be6fe58dad94815f
Source noteuspto-grants-2012_06