Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propionitrile | HCID 7854 | — |
| Reactant | 4-chloro-5-iodo-2-methylthio-6-trifluoromethylpyrimidine | HCID 12151419 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Product | HCID 12151210 | HCID 12151210 | — |
Reaction Steps
4-Chloro-5-iodo-2-methylthio-6-trifluoromethylpyrimidine (5.00 g) was dissolved in propionitrile (125 ml) and 4-(dimethylamino)-pyridine (1.81 g) was added at room temperature with stirring. After several minutes, precipitates appeared, however, it was stirred over night at room temperature. The slurry was cooled to ice bath temperature, and then added sodium cyanide (1.04 g) water (10 ml) solution. The mixture was warmed to room temperature and stirred 3 hr. The reaction mixture was added water and extracted with ethyl acetate. The ethyl acetate layer was washed with water and brine, respectively and dried over magnesium sulfate. The solvent was removed under reduced pressure. The residue was purified by silica get column chromatography (hexane-ethyl acetate) to give 4-cyano-5-iodo-2-methylthio-6-trifluoromiethylpyrimidine (2.56 g) as yellow solid, mp 68-69° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06818631B1 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-30b9ecbffa8249bfb88cdb22d480dbfb |
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| Source note | uspto-grants-2004_11 |
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