HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1643500Erstellt: 25. Oktober 2026
Dimethyl Sulfoxide → Biphenyl-2-ylcarbamic Acid 1-[2-(3-formylbenzylcarbamoyl)ethyl]piperidin-4-yl Ester
https://huagongshe.com/reaction/1643500
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethyl Sulfoxide | HCID 679 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | Sulfur trioxide-pyridine | HCID 168533 | — |
| Edukt | Biphenyl-2-ylcarbamic acid 1-[2-(3-hydroxymethylbenzylcarbamoyl)ethyl]piperidin-4-yl Ester | HCID 59340333 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Biphenyl-2-ylcarbamic Acid 1-[2-(3-formylbenzylcarbamoyl)ethyl]piperidin-4-yl Ester | HCID 59340336 | — |
Reaktionsschritte
To a flask was added biphenyl-2-ylcarbamic acid 1-[2-(3-hydroxymethylbenzyl carbamoyl)ethyl]piperidin-4-yl ester (0.33 g, 0.68 mmol; prepared as described in Preparation 12), DCM (5 mL), DIPEA (0.47 mL, 2.7 mol) and DMSO (0.2 mL, 2.7 mol). Using an ice bath, the mixture was cooled to about −10° C. and sulfur trioxide pyridine-complex (0.32 g, 2.0 mol) was added. The reaction was stirred at −10° C. for 0.75 hour. Before removing the ice-bath, the reaction was quenched by adding water (5 mL). The aqueous layer was separated and the organic layer was washed with water (2×5 mL), 1.0N NaHSO4(aq) (2×5 mL), 1.0N NaHCO3(aq) (1×5 mL) and brine (0.5 L) and then dried over MgSO4 and filtered to provide the title compound which was used without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08119796B2 |
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| Quelldatensatz | uspto-grants-2012_02 |
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| ORD ID | ord-bc16a827c36c4d2787d08a014512d8a1 |
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| Quellennotiz | uspto-grants-2012_02 |
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