HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 935Erstellt: 23. Oktober 2026
Dimethylformamide → cis-N-[1-[3-(4-Fluorophenoxy)propyl]-3-methoxy-4-piperidinyl]-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamide
https://huagongshe.com/de/reaction/935
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 1-(3-Bromopropoxy)-4-fluorobenzene | HCID 260004 | — |
| Edukt | cis-N-(3-Methoxy-4-piperidinyl)-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamide | HCID 69232145 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | cis-N-[1-[3-(4-Fluorophenoxy)propyl]-3-methoxy-4-piperidinyl]-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamide | HCID 69229498 | 91,8% |
Reaktionsschritte
A mixture comprising 0.10 g of the cis-N-(3-methoxy-4-piperidinyl)-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamide, 0.07 g of 3-(4-fluorophenoxy)propyl bromide, 0.20 g of triethylamine and 10 ml of DMF was stirred at 50° C. for 2 hours and cooled. Ethyl acetate was poured into the resulting mixture. The obtained mixture was washed with water thrice, dried over magnesium sulfate, and freed from the solvent. The residue was purified by silica gel column chromatography (5% methanol/dichloromethane) to give 0.13 g of the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05723472 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-e90e3b33efd8427982a8d67e8d113a2f |
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| Quellennotiz | uspto-grants-1998_03 |
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