HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 913069Erstellt: 25. Oktober 2026
Acetic Acid → N-{3-[1-(4-Chloro-3-ethoxy-benzyl)-piperidin-4-ylamino]-phenyl}-acetamide
https://huagongshe.com/reaction/913069
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Sodium cyanoborohydride | HCID 5003444 | — |
| Edukt | 4-Chloro-3-ethoxybenzaldehyde | HCID 54775642 | — |
| Edukt | N-[3-(Piperidin-4-ylamino)-phenyl]-acetamide dihydrochloride | HCID 67400427 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | N-{3-[1-(4-Chloro-3-ethoxy-benzyl)-piperidin-4-ylamino]-phenyl}-acetamide | HCID 24854968 | 12,4% |
Reaktionsschritte
To a solution of N-[3-(piperidin-4-ylamino)-phenyl]-acetamide dihydrochloride (61.2 mg, 0.2 mmol, 1.0 equiv; intermediate B1), acetic acid (60.1 mg, 1.0 mmol, 5.0 equiv) and triethylamine (40.5 mg, 0.4 mmol, 2.0 equiv) in ethanol (1 mL) was added 4-chloro-3-ethoxy-benzaldehyde (46.1 mg, 0.25 mmol, 1.25 equiv; intermediate E2, vide infra) and the mixture stirred at 50° C. After 1 h, sodium cyanoborohydride (15.1 mg, 0.24 mmol, 1.2 equiv), dissolved in ethanol (1 mL), was added and the mixture stirred at 50° C. over night. Removal of the solvent under reduced pressure and purification by preparative HPLC on reversed phase eluting with a gradient of acetonitrile/water provided 10.0 mg (12%) of the title compound. MS (ISP): 402.3 [M+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08026255B2 |
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| Quelldatensatz | uspto-grants-2011_09 |
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| ORD ID | ord-19cd267097e24998868990e89a31b09b |
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| Quellennotiz | uspto-grants-2011_09 |
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