HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11125Erstellt: 25. Oktober 2026
Azido(trimethyl)stannane → HCID 178418841, Verbindung
https://huagongshe.com/reaction/11125
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Azido(trimethyl)stannane | HCID 5104973 | — |
| Edukt | 3-(4-(2-Chlorophenyl)-9-hydroxy-1,3-dioxo-2,3-dihydropyrrolo[3,4-c]carbazol-6(1H)-yl)propanenitrile | HCID 24884697 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Lösungsmittel | Dimethylformamide toluene | HCID 21735183 | — |
| Produkt | HCID 178418841 | HCID 178418841 | 72,2% |
Reaktionsschritte
To a solution of nitrile (238) (0.68 g, 1.63 mmol) prepared as described in example 98 in toluene/dimethylformamide (5:1, 120 mL) was added azidotrimethyl tin (0.67 g, 3.26 mmol). The resulting solution was heated at reflux for 24 hours before a further portion of azidotrimethyl tin (0.34 g, 1.63 mmol) was added. After a further 24 hours at reflux the reaction was diluted with water and extraction with ethyl acetate. The organic phase was dried, the drying agent was removed and the solution was concentrated to dryness. Chromatography on silica eluting with ethyl acetatelhexane (3:1) to ethyl acetate/methanol (9:1), followed by crystallization from ethyl acetate/hexane, gave tetrazole (272) (0.54 g, 72%) as an orange powder, mp 230–234° C. (dec). 1H NMR δ [(CD3)2SO] 11.06 (br s, 1H), 9.37 (br s, 1H), 8.36 (d, J=2.4 Hz, 1H), 7.61 (s, 1H), 7.56 (m, 1H), 7.48 (m, 4H), 7.10 (dd, J=8.8, 2.4 Hz, 1H), 4.82 (t, J=6.9 Hz, 2H), 3.32 (obscured t, J=6.9 Hz, 2H). Found: C, 52.69; H, 4.05; N, 15.91. C23H15ClN6O3.31/2H2O requires: C, 52.93; H, 4.25; N, 16.09.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07094798B1 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-48da5ed2f8704646a3a54504d181f110 |
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| Quellennotiz | uspto-grants-2006_08 |
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