HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1925163Erstellt: 26. Oktober 2026
Potassium Iodide → (6-(2-([1,2,4]Triazolo[4,3-a]pyridin-3-yl)propan-2-yl)imidazo[1,2-b]pyridazin-2-yl)(cyclopropyl)methanone
https://huagongshe.com/reaction/1925163
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Potassium Iodide | HCID 4875 | — |
| Edukt | Sodium Phosphate, Dibasic | HCID 24203 | — |
| Edukt | N-(2-bromoacetyl)cyclopropanecarboxamide | HCID 59233013 | — |
| Edukt | HCID 66633764 | HCID 66633764 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Produkt | (6-(2-([1,2,4]Triazolo[4,3-a]pyridin-3-yl)propan-2-yl)imidazo[1,2-b]pyridazin-2-yl)(cyclopropyl)methanone | HCID 59233066 | 27,6% |
Reaktionsschritte
A mixture of 6-(2-([1,2,4]triazolo[4,3-a]pyridin-3-yl)propan-2-yl)pyridazin-3-amine 2,2,2-trifluoroacetate (50 mg, 0.136 mmol), N-(2-bromoacetyl)cyclopropanecarboxamide (28.0 mg, 0.136 mmol), sodium hydrogenphosphate (57.8 mg, 0.407 mmol), and potassium iodide (22.54 mg, 0.136 mmol) in DMA (Volume: 1160 μl) was heated in a microwave on high absorbance for 1 hr at 100° C. The reaction was purified by preparative LCMS to provide the title compound, (6-(2-([1,2,4]triazolo[4,3-a]pyridin-3-yl)propan-2-yl)imidazo[1,2-b]pyridazin-2-yl)(cyclopropyl)methanone (54, 13 mg, 26%) as a TFA salt. 1H NMR (400 MHz, DMSO-d6) δ ppm 0.81 (d, J=6.06 Hz, 4 H) 1.87-2.00 (m, 7 H) 6.92-6.97 (m, 1 H) 7.12 (d, J=9.60 Hz, 1 H) 7.55 (dd, J=8.97, 6.69 Hz, 1 H) 7.87-8.01 (m, 3H) 8.04 (s, 1 H) 11.16 (s, 1 H). ESI-MS:m/z 362.1 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08178534B2 |
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| Quelldatensatz | uspto-grants-2012_05 |
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| ORD ID | ord-63d24aa437f84b4c8592ef1ef52d45ba |
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| Quellennotiz | uspto-grants-2012_05 |
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