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HRID 42779Erstellt: 24. Oktober 2026
Nitrogen → 4-(2-Methyl-[1,3]dioxolan-2-yl)-2-(4-nitro-[1,2,3]triazol-2-ylmethyl)-pyridine
https://huagongshe.com/de/reaction/42779
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Nitrogen | HCID 947 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 4-nitro-2H-1,2,3-triazole | HCID 278150 | — |
| Edukt | Methanesulfonic acid 4-(2-methyl-[1,3]dioxolan-2-yl)-pyridin-2-ylmethyl ester | HCID 86649481 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 4-(2-Methyl-[1,3]dioxolan-2-yl)-2-(4-nitro-[1,2,3]triazol-2-ylmethyl)-pyridine | HCID 67363839 | — |
Reaktionsschritte
In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of methanesulfonic acid 4-(2-methyl-[1,3]dioxolan-2-yl)-pyridin-2-ylmethyl ester (315 mg, 1.15 mmol) in DMF (2.0 mL) was added to a solution of 4-nitro-2H-[1,2,3]triazole (120 mg, 1.05 mmol) in DMF (2.0 mL) pre-treated for 30 min with DIPEA (0.36 mL, 2.10 mmol) and the reaction mixture was stirred for 48 h at 50° C. Water (10 mL), followed by EA (10 mL) were added. The aq. layer was extracted with EA (10 mL) and the combined org. extracts were dried over NaSO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (5:1 to 1:4 hept-EA) gave the title compound as a pale yellow solid: TLC:rf (1:2 hept-EA)=0.24. LC-MS-conditions 02: tR=0.89 min, [M+H]+=292.27.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08536209B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-f4592e37c3ff4ed592b3f7d14287cba8 |
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| Quellennotiz | uspto-grants-2013_09 |
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