HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331887Generated: October 25, 2026
Dimethyl Sulfoxide → Methyl 6-(((5-methyl-3-phenylisoxazol-4-yl)methyl)amino)nicotinate
https://huagongshe.com/reaction/331887
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methyl 6-chloropyridine-3-carboxylate | HCID 254249 | — |
| Reactant | (5-Methyl-3-phenyl-4-isoxazolyl)-methylamine | HCID 59594513 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 6-(((5-methyl-3-phenylisoxazol-4-yl)methyl)amino)nicotinate | HCID 68443539 | 46.1% |
Reaction Steps
A mixture of (5-methyl-3-phenyl-4-isoxazolyl)-methylamine (200 mg, 1.06 mmol), methyl 6-chloronicotinate (182 mg, 1.06 mmol), N,N-diisopropyl ethyl amine (364 μL, 2.13 mmol) and DMSO (2 mL) was heated in the microwave to 160° C. for 0.5 h. It was diluted with ethyl acetate (8 mL) and washed with aqueous sodium carbonate (saturated, 8 mL), water (8 mL) and brine (8 mL). The combined aqueous layers were extracted with ethyl acetate (10 mL) and the combined organic layers were dried over sodium sulfate. Concentration and purification by chromatography (SiO2, heptane:ethyl acetate=100:0 to 50:50) afforded the title compound (158 mg, 46%) as a light yellow oil. MS: m/e=324.3 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877782B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-9da42129b43e401b86bddb41c49ff500 |
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| Source note | uspto-grants-2014_11 |
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