HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 40035Erstellt: 24. Oktober 2026
Boron tribromide → 1-Benzyl-N-(3,4-difluorobenzyl)-6-hydroxy-2-isopropyl-1H-indole-3-carboxamide
https://huagongshe.com/de/reaction/40035
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Boron tribromide | HCID 25134 | — |
| Edukt | 1-Benzyl-N-(3,4-difluorobenzyl)-2-isopropyl-6-methoxy-1H-indole-3-carboxamide | HCID 44159276 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 1-Benzyl-N-(3,4-difluorobenzyl)-6-hydroxy-2-isopropyl-1H-indole-3-carboxamide | HCID 25160740 | — |
Reaktionsschritte
To a solution of 1-benzyl-N-(3,4-difluorobenzyl)-2-isopropyl-6-methoxy-1H-indole-3-carboxamide (Compound 7, 452 mg, 1.0 mmol) in CH2Cl2 (20 ml) at 0° C. was added BBr3 (1.0 M in CH2Cl2, 3.0 ml, 3.0 mmol) dropwise. The reaction was stirred for 1 h at 0° C. and 1 h at room temperature, quenched with ice, extracted with EtOAc, the organic layer was washed with brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified by chromatography on silica gel (0→50% EtOAc-hexanes) to yield the title compound as a yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08524917B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-25f4e497f4f04357950d61bfc102aa0e |
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| Quellennotiz | uspto-grants-2013_09 |
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