HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373777Generated: October 31, 2026
Hydrochloric Acid → HCID 136148285, compound
https://huagongshe.com/reaction/1373777
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | 1-(4-Fluorophenyl)-2-[2-(methylsulfanyl)pyrimidin-4-yl]ethan-1-one | HCID 11747416 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Product | HCID 136148285 | HCID 136148285 | — |
Reaction Steps
To a suspension of 1-(4-fluorophenyl)-2-(2-(methylthio)pyrimidin-4-yl)ethanone, 73 (1.0 g) in ethanol (20 mL) at −10° C., under an atmosphere of nitrogen, is added dropwise t-butyl nitrite (0.5 mL) followed by hydrogen chloride in n-propanol (2.5 to 3 N, 0.6 mL) while maintaining the temperature below −5° C. Once the addition is complete, the solution is allowed to warm to room temperature with stirring and after 2 h the solvent is evaporated and the residue partitioned between saturated aqueous sodium hydrogen carbonate and ethyl acetate. The layers are separated; the aqueous phase is extracted with ethyl acetate and the combined organic phases dried over sodium sulfate. Filtration and evaporation of the solvent affords the title compound, 74 (1.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07163945B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-fbc59ea81780425cafb1d95e46094d80 |
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| Source note | uspto-grants-2007_01 |
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