HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2065038Erstellt: 26. Oktober 2026
Bromide ion → 2-(2-Methyl-[1,3]dioxolan-2-yl)-4-(3-nitro-pyrazol-1-ylmethyl)-thiazole
https://huagongshe.com/reaction/2065038
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Bromide ion | HCID 259 | — |
| Edukt | Nitrogen | HCID 947 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 3-Nitropyrazole | HCID 123419 | — |
| Edukt | 4-Chloromethyl-2-(2-methyl-[1,3]dioxolan-2-yl)-thiazole | HCID 66928813 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-(2-Methyl-[1,3]dioxolan-2-yl)-4-(3-nitro-pyrazol-1-ylmethyl)-thiazole | HCID 66929202 | — |
Reaktionsschritte
In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 4-chloromethyl-2-(2-methyl-[1,3]dioxolan-2-yl)-thiazole (174 mg, 0.79 mmol) in acetone (2.0 mL) was added to a solution of 5-nitro-1H-pyrazole (90 mg, 0.79 mmol) in acetone (2.0 mL). K2CO3 (330 mg, 2.38 mmol) followed by TBA bromide (51 mg, 0.16 mmol) were added and the reaction mixture was stirred at rt overnight. Water (10 mL) and EA (10 mL) were added. The aq. layer was extracted with EA (10 mL) and the combined org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (1:1 hept-EA) gave the title compound as a pale yellow oil. TLC: rf (1:1 hept-EA)=0.29. LC-MS-conditions 02: tR=0.89 min, [M+H]+=297.23.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08288419B2 |
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| Quelldatensatz | uspto-grants-2012_10 |
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| ORD ID | ord-847dc52d889d4f81ac88a42543f6fa0e |
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| Quellennotiz | uspto-grants-2012_10 |
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