HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2246835Erstellt: 26. Oktober 2026
Dimethyl Sulfoxide → 10-[(2'-Methoxy-1,1'-biphenyl-4-yl)carbonyl]-n-[(1-methyl-1h-pyrrol-2-yl)methyl]-10,11-dihydro-5h-pyrrolo[2,1-c][1,4]benzodiazepine-3-carboxamide
https://huagongshe.com/reaction/2246835
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethyl Sulfoxide | HCID 679 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | (1-methyl-1H-pyrrol-2-yl)methanamine | HCID 2776207 | — |
| Edukt | 2,2,2-trichloro-1-{10-[(2'-methoxy-1,1'-biphenyl-4-yl)carbonyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-3-yl}ethanone | HCID 16038407 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 10-[(2'-Methoxy-1,1'-biphenyl-4-yl)carbonyl]-n-[(1-methyl-1h-pyrrol-2-yl)methyl]-10,11-dihydro-5h-pyrrolo[2,1-c][1,4]benzodiazepine-3-carboxamide | HCID 11999853 | 40,3% |
Reaktionsschritte
To a suspension of 2,2,2-trichloro-1-{10-[(2′-methoxy-1,1′-biphenyl-4-yl)carbonyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-3-yl}ethanone of Example 1 (1.175 g, 2.17 mmole) in acetonitrile (15 mL) was added (1-methyl-1H-pyrrol-2-yl)methylamine (0.263 g, 2.38 mmole) followed by dimethylsulfoxide (0.710 g, 9.06 mmole) and triethylamine (0.400 g, 4 mmole). The mixture was heated under nitrogen at 80° C. for 4 hours. The solvent was removed in vacuo, and the residue was flash chromatographed on silica Merck-60 using a gradient of 0-25% of ethyl acetate in dichloromethane, to provide a yellow foam that yields a solid (0.464 g) upon treatment with ethyl acetate and hexane, mp 148-150° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07687623B2 |
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| Quelldatensatz | uspto-grants-2010_03 |
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| ORD ID | ord-8a4f9b1cfbc84c51972a44d3dc84ab72 |
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| Quellennotiz | uspto-grants-2010_03 |
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