HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1011903Erstellt: 26. Oktober 2026
Dicyclohexylcarbodiimide → [5-(3-benzofuran-2-yl-phenyl)-1,4-dimethyl-1H-pyrazol-3-yl]-[4-(2-hydroxy-ethyl)-[1,4]diazepan-1-yl]-methanone
https://huagongshe.com/reaction/1011903
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Edukt | 2-(1,4-Diazepan-1-yl)ethan-1-ol | HCID 2736550 | — |
| Edukt | 5-(3-benzofuran-2-yl-phenyl)-1,4-dimethyl-1H-pyrazole-3-carboxylic acid | HCID 67314297 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | [5-(3-benzofuran-2-yl-phenyl)-1,4-dimethyl-1H-pyrazol-3-yl]-[4-(2-hydroxy-ethyl)-[1,4]diazepan-1-yl]-methanone | HCID 67314874 | 40% |
Reaktionsschritte
To a suspension of 0.060 g (0.18 mmol) of 5-(3-benzofuran-2-yl-phenyl)-1,4-dimethyl-1H-pyrazole-3-carboxylic acid in 2 ml of CH2Cl2 was added 0.031 g (0.22 mmol) of 2-(1,4-diazepan-1-yl)ethan-1-ol, diluted in 1.7 ml of CH2Cl2. This solution was treated at 0° C. with 0.048 g (0.23 mmol) of DCC. The reaction was allowed to warm up over night to RT, then partitioned between aqueous saturated NaHCO3/EtOAc (3×). The organic phases were washed with aqueous saturated NaHCO3, dried (Na2SO4) and evaporated. The residue was suspended in EtOAc and filtered to remove the DCC urea. Purification by flash chromatography (SiO2—NH2, n-heptane/EtOAc 1:4) gave 0.033 g (39%) of [5-(3-benzofuran-2-yl-phenyl)-1,4-dimethyl-1H-pyrazol-3-yl]-[4-(2-hydroxy-ethyl)-[1,4]diazepan-1-yl]-methanone as white oil. MS: 459.3 (MH+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07977358B2 |
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| Quelldatensatz | uspto-grants-2011_07 |
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| ORD ID | ord-e741a131714d448195f6d2f35319d480 |
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| Quellennotiz | uspto-grants-2011_07 |
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