HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 448035Erstellt: 24. Oktober 2026
5-Chloro-2-fluorobenzoyl chloride → (2Z)-2-(3-butyl-4-methyl-1,3-thiazol-2(3H)-ylidene)-1-(5-chloro-2-fluorophenyl)ethanone
https://huagongshe.com/de/reaction/448035
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 5-Chloro-2-fluorobenzoyl chloride | HCID 2773604 | — |
| Edukt | 3-Butyl-2,4-dimethylthiazol-3-ium iodide | HCID 69165109 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Dimethyl sulfoxide methanol | HCID 22036561 | — |
| Produkt | (2Z)-2-(3-butyl-4-methyl-1,3-thiazol-2(3H)-ylidene)-1-(5-chloro-2-fluorophenyl)ethanone | HCID 69321127 | — |
Reaktionsschritte
In a 20 mL vial a solution of 3-butyl-2,4-dimethylthiazol-3-ium iodide (47.92 mg, 0.16 mmol) dissolved in CH2Cl2 (0.5 mL) was added, followed by the addition of DMAP (49.24 mg, 0.40 mmol) dissolved in CH2Cl2 (0.8 mL). Then, to the solution was added 5-chloro-2-fluorobenzoyl chloride (30.9 mg, 0.16 mmol) dissolved in CH2Cl2 (0.5 mL). The vial was capped and shaken overnight at room temperature. The residue was dissolved in 1:1 DMSO/MeOH and purified by reverse phase HPLC using a method analogous to that described in Example 53 to provide the title compound. 1H NMR (500 MHz, DMSO-d6/D2O) δ ppm 0.95 (t, 3 H) 1.31-1.41 (m, 2 H) 1.57-1.77 (m, 2 H) 2.28-2.34 (m, 3 H) 3.95-4.02 (m, 2 H) 6.37-6.41 (m, 1 H) 6.55-6.68 (m, 1 H) 7.28-7.35 (m, 1 H) 7.48-7.54 (m, 1 H) 7.76-7.80 (m, 1 H); MS (ESI) positive ion 326 (M+H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08481574B2 |
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| Quelldatensatz | uspto-grants-2013_07 |
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| ORD ID | ord-44b24e79dbd443248ff86fd9a24d2e62 |
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| Quellennotiz | uspto-grants-2013_07 |
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