HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 855418Erstellt: 25. Oktober 2026
1-Hydroxybenzotriazole → HCID 86603103, Verbindung
https://huagongshe.com/reaction/855418
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Edukt | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Edukt | (4-Tert-butyl-benzyl)-[2-(4-fluoro-phenyl)-ethyl]-amine | HCID 29280418 | — |
| Edukt | 4-Chloro-1H-indole-7-carboxylic acid | HCID 69346850 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | HCID 86603103 | HCID 86603103 | 65% |
Reaktionsschritte
To a solution of 64 mg (0.33 mmol) of 4-chloro-1H-indole-7-carboxylic acid in 2 ml DCM 50 mg of HOBT (0.33 mmol) were added and the reaction mixture was stirred for 15 min at rt under nitrogen. 85 mg (0.3 mmol) of (4-tert-butyl-benzyl)-[2-(4-fluoro-phenyl)-ethyl]-amine in 1 ml DCM were added and then 63 mg (0.33 mmol) of EDC.HCl. The reaction mixture was stirred over night at rt to yield a slight turbid yellow solution. The solvent was evaporated and the residue was dissolved in 1,2-dichloro ethane. The reaction mixture was stirred at reflux for 3 h. The solvent was evaporated and the residue was purified by column chromatography (25 g silica gel, heptane/EtOAc 7:3) to yield 90 mg (65%) product as a light yellow viscous oil. MS (ISP) 463.4 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07259183B2 |
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| Quelldatensatz | uspto-grants-2007_08 |
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| ORD ID | ord-fa923246e7d54064af09f388dd795d99 |
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| Quellennotiz | uspto-grants-2007_08 |
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