HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 402815Erstellt: 25. Oktober 2026
6-Methoxy-1H-indole-3-carboxaldehyde → 1-cyclopropyl-6-methoxy-1H-indole-3-carbaldehyde
https://huagongshe.com/reaction/402815
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 6-Methoxy-1H-indole-3-carboxaldehyde | HCID 907214 | — |
| Edukt | Cyclopropylboronic acid | HCID 2760897 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 1-cyclopropyl-6-methoxy-1H-indole-3-carbaldehyde | HCID 86685271 | 40,9% |
Reaktionsschritte
Dihydroxo-bis[N,N,N′,N′-tetramethylenediamine)copper (II) chloride (26 mg, 0.057 mmol) was added to a stirred room temperature mixture of 6-methoxy-1H-indole-3-carbaldehyde (100 mg, 0.568 mmol) and cyclopropylboronic acid (98 mg, 1.13 mmol) in dichloromethane (3 mL). Molecular sieves (4 A°, 100 mg) were added and the mixture was stirred under oxygen at room temperature for 48 hours. The reaction mixture was filtered over a pad of silica gel, washed with dichloromethane, partitioned between dichloromethane (10 mL) and 10% ammonium hydroxide (2×10 mL). The organic layer was washed with water (10 mL) and brine (10 mL). The organic layer was dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography (Biotage 25 M), eluting with EtOAc/hexanes to give the title compound (50 mg) as a oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08742110B2 |
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| Quelldatensatz | uspto-grants-2014_06 |
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| ORD ID | ord-bd40677a9d6c4dbc9e8ae4271c401b3c |
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| Quellennotiz | uspto-grants-2014_06 |
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