HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1990796Erstellt: 25. Oktober 2026
Acetic Acid → Benzothiazol-2-yl-[1-(2-ethoxy-naphthalen-1-ylmethyl)-piperidin-4-yl]-amine
https://huagongshe.com/reaction/1990796
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 2-Ethoxynaphthalene-1-carbaldehyde | HCID 88099 | — |
| Edukt | Sodium cyanoborohydride | HCID 5003444 | — |
| Edukt | N-(Piperidin-4-yl)-1,3-benzothiazol-2-amine | HCID 14575274 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | Benzothiazol-2-yl-[1-(2-ethoxy-naphthalen-1-ylmethyl)-piperidin-4-yl]-amine | HCID 86607625 | 8% |
Reaktionsschritte
To a solution of benzothiazol-2-yl-piperidin-4-yl-amine (23.3 mg, 0.1 mmol, 1.0 equiv) and 2-ethoxy-naphthalene-1-carbaldehyde (commercially available, 24.0 mg, 0.12 mmol, 1.2 equiv) in ethanol (2 mL) was added diisopropylethylamine (23.42 μL, 25.9 mg, 0.2 mmol, 2.0 equiv) and acetic acid (18.0 mg, 0.3 mmol, 3.0 equiv) and the mixture stirred at 40° C. After 1 h, sodium cyano borohydride (7.54 mg, 0.12 mmol, 1.2 equiv) was added and the mixture stirred at 40° 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 3.3 mg (8%) of the title compound. MS (ESI): 418.4 [M+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07645753B2 |
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| Quelldatensatz | uspto-grants-2010_01 |
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| ORD ID | ord-8ee5054967184bad9481d5be680ac808 |
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| Quellennotiz | uspto-grants-2010_01 |
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