HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 902976Erstellt: 24. Oktober 2026
Dimethylformamide → {3-[7-(3-Diethylamino-prop-1-ynyl)-5,5-dioxo-5H-5lambda6-dibenzothiophen-3-yl]-prop-2-ynyl}-diethylamine
https://huagongshe.com/de/reaction/902976
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Dietylaminopropin | HCID 20010 | — |
| Edukt | 3,7-Dibromo-dibenzothiophene 5,5-dioxide | HCID 4071898 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Katalysator | HCID 178418903 | HCID 178418903 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | {3-[7-(3-Diethylamino-prop-1-ynyl)-5,5-dioxo-5H-5lambda6-dibenzothiophen-3-yl]-prop-2-ynyl}-diethylamine | HCID 67163580 | 82% |
Reaktionsschritte
A mixture of 3,7-dibromodibenzothiophene 5,5-dioxide (0.33 g, 0.88 mmol; see J. Med. Chem. 1978, 21, 1084), 3-diethylamino-1-propyne (0.5 mL, 3.4 mmol; Lancaster), triethylamine (0.6 mL, 4.2 mmol; Acros), dichlorobis(triphenylphosphino)palladium(II) (Cl2Pd(PPh3)2; 25 mg, 0.035 mmol; Aldrich), and copper(I) iodide (38 mg, 0.20 mmol; Aldrich) in DMF (10 mL) was heated to 65° C. for 60 h. The reaction mixture was diluted with EtOAc, washed with water and brine, and dried over Na2SO4. The residue was purified by chromatography (16 g silica gel, 2-7% gradient MeOH in CH2Cl2to afford the title compound (0.31 g, 0.71 mmol, 82% yield): MS (DCl/NH3) m/z 435 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07365193B2 |
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| Quelldatensatz | uspto-grants-2008_04 |
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| ORD ID | ord-b40e7644f83343a7a88643ebda83fd87 |
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| Quellennotiz | uspto-grants-2008_04 |
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