HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1046554Erstellt: 25. Oktober 2026
Dichloromethane → Tert-butyl 2-(4-((2,2-difluorobenzo[d][1,3]dioxole-5-carboxamido)methyl)piperidin-1-yl)ethylcarbamate
https://huagongshe.com/reaction/1046554
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 2,2-Difluoro-1,3-benzodioxole-5-carbonyl chloride | HCID 2774064 | — |
| Edukt | Tert-butyl 2-(4-(aminomethyl)piperidin-1-yl)ethylcarbamate | HCID 57993236 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | Tert-butyl 2-(4-((2,2-difluorobenzo[d][1,3]dioxole-5-carboxamido)methyl)piperidin-1-yl)ethylcarbamate | HCID 57993507 | — |
Reaktionsschritte
A solution of tert-butyl 2-(4-(aminomethyl)piperidin-1-yl)ethylcarbamate (50 mg, 0.19 mmol) and TEA (135 μL, 0.972 mmol) in a mixture of 1:1 CH2Cl2:THF (2.5 mL) was treated with 2,2-difluorobenzo[d][1,3]dioxole-5-carbonyl chloride (51 mg, 0.23 mmol). The resulting solution was stirred overnight, then transferred to a test tube containing saturated aqueous NaHCO3 (4 mL) and EtOAc (4 mL). The biphasic mixture was mixed vigorously and allowed to separate for 15 minutes. After separation, the mixture was cooled to −20° C. until the aqueous layer was frozen. The organic layer was then poured off and the solvent was removed under reduced pressure at 50° C. The resulting residue was purified by HiTOPs.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08569344B2 |
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| Quelldatensatz | uspto-grants-2013_10 |
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| ORD ID | ord-b96866da95ac4e5cbdba008aa014b413 |
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| Quellennotiz | uspto-grants-2013_10 |
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