Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 1-(3,4-Dimethoxy-5-nitrophenyl)-3-(dimethylamino)prop-2-en-1-one | HCID 67036875 | — |
| Reactant | HCID 67359629 | HCID 67359629 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 68704968 | HCID 68704968 | — |
Reaction Steps
A stirred suspension of 1-(3,4-dimethoxy-5-nitro-phenyl)-3-dimethylamino-propen-1-one (0.28 g, 1.0 mmol), 2-(trifluoromethyl)nicotinimidamide (0.283 g, 1.5 mmol) and potassium tert-butoxide (0.17 g, 1.5 mmol) in absolute ethanol (5 mL) was heated to 80° C. in a sealed tube for one hour and then allowed to cool to room temperature. The mixture was poured onto cold water (100 mL) and the resulting precipitate was filtered off, washed with water and dried to give 4-(3,4-dimethoxy-5-nitrophenyl)-2-(2-(trifluoromethyl)pyridin-3-yl)pyrimidine, 0.296 g (73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08536203B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-c82858482f554217a9a3a577c3255b0c |
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| Source note | uspto-grants-2013_09 |
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