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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktSodium BicarbonateHCID 516892—
Edukt2,2-Difluoro-1,3-benzodioxole-5-carbonyl chlorideHCID 2774064—
EduktTert-butyl 2-(4-(aminomethyl)piperidin-1-yl)ethylcarbamateHCID 57993236—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
ProduktTert-butyl 2-(4-((2,2-difluorobenzo[d][1,3]dioxole-5-carboxamido)methyl)piperidin-1-yl)ethylcarbamateHCID 57993507—

Reaktionsbedingungen

Temperatur-20 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08569344B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-b96866da95ac4e5cbdba008aa014b413
Quellennotizuspto-grants-2013_10