HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1045614Erstellt: 25. Oktober 2026
Potassium Phosphate, Tribasic → HCID 59368187, Verbindung
https://huagongshe.com/reaction/1045614
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Edukt | L-Proline | HCID 145742 | — |
| Edukt | 9-Chloro-3-methyl-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole | HCID 68558507 | — |
| Edukt | (1-Bromoprop-1-en-2-yl)-3,4-dichlorobenzene | HCID 86635503 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | HCID 59368187 | HCID 59368187 | — |
Reaktionsschritte
9-Chloro-3-methyl-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole (74 mg, 0.31 mmol) was dissolved in DMF (5 mL). Copper (I) iodide (6 mg, 0.032 mmol), L-proline (7 mg, 0.063 mmol) and K3PO4 (134 mg, 0.63 mmol) were added and the reaction mixture was stirred for 10 min. at RT. 4-(1-Bromoprop-1-en-2-yl)-1,2-dichlorobenzene (100 mg, 0.378 mmol) was added dropwise and the reaction mixture was purged with nitrogen. The reaction mixture was heated at 80° C. for overnight (prolonged heating in some cases was required). The DMF was evaporated under reduced pressure, the residue was diluted with water and the solid was filtered. The solid material was purified by silica gel chromatography (100-200 mesh). Yield: 74 mg. 1HNMR (CD3OD, TFA salt) δ (ppm): 7.82 (d, 1H), 7.62 (d, 2H), 7.57 (s, 1H), 7.18 (d, 2H), 7.10 (d, 1H), 3.78 (m, 2H), 3.40 (m, 4H), 3.20 (m, 2H), 3.06 (s, 3H), 1.90 (s, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08569287B2 |
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| Quelldatensatz | uspto-grants-2013_10 |
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| ORD ID | ord-57c23ce9e98a4ec8b95e073f485d40b9 |
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| Quellennotiz | uspto-grants-2013_10 |
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