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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Butanenitrile, 3-imino- | HCID 70698 | — |
| Reactant | 4-Hydrazinyl-6-(methylthio)pyrimidine | HCID 13519855 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Methyl-2-(6-methylsulfanyl-pyrimidin-4-yl)-2H-pyrazol-3-ylamine | HCID 59173368 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08202876B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-e8f9c9326c874781be6fe58dad94815f |
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| Source note | uspto-grants-2012_06 |
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