Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 4-Pyridinemethanamine | HCID 77317 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22139640 | HCID 22139640 | 70.7% |
Reaction Steps
To a cold (ice-water bath) solution of 4-picolylamine (1070 gr, 9.9 mol) in methanol (3 l) was added dropwise acetic anhydride (1400 gr, 13.7 mol). During addition the reaction temperature was kept between 10 and 30° C. When the addition of the reagent was complete the reaction mixture was left overnight at room temperature. Iodomethane (800 ml, 24.8 mol) was added to the reaction mixture which was cooled with water bath, under nitrogen atmosphere. During addition the reaction temperature was kept below 25° C. When the addition was complete, the reaction mixture was protected from light and left at room temperature overnight The excess iodomethane was evaporated, crystallization was induced, the reaction mixture was cooled (ice bath) and isopropanol (1.5 l) was added. The reaction mixture was left at −30° C. overnight, the precipitate was filtered off, washed with isopropanol and dried. 4-(Acetaminomethyl)-1-methyl-pyridinium iodide (2043 gr, 7 mol) was obtained as yellow powder (71% yield). 1H-NMR (D2O) δ 2.10 (s, CH3CO), 4.32 (s, CH3N+), 4.63 (s, CH2NHCO), 7.89 (d, j=6.6 Hz, 2H), 8.67 (d, j=6.6 Hz, 2H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07439251B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-ca82a778b30346b69102abe4da54eaf0 |
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| Source note | uspto-grants-2008_10 |
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