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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2167033Erstellt: 24. Oktober 2026

2-(Pyridin-3-yl)ethan-1-amine → {2-[(9R)-9-(pyridin-2-yl)-6-oxaspiro[4.5]decan-9-yl]ethyl}[2-(pyridin-3-yl)ethyl]amine

https://huagongshe.com/de/reaction/2167033

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(Pyridin-3-yl)ethan-1-amineHCID 854051—
EduktSodium borohydrideHCID 4311764—
Edukt2-[(9R)-9-pyridin-2-yl-6-oxaspiro[4.5]decan-9-yl]acetaldehydeHCID 86671427—
KatalysatorMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
Produkt{2-[(9R)-9-(pyridin-2-yl)-6-oxaspiro[4.5]decan-9-yl]ethyl}[2-(pyridin-3-yl)ethyl]amineHCID 68314495—

Reaktionsschritte

To a solution of 2-[(9R)-9-(pyridin-2-yl)-6-oxaspiro[4.5]decan-9-yl]acetaldehyde (50 mg, 0.19 mmole), 5 mL DCM and NA2SO4 (134 mg, 0.95 mmole) was added 2-(pyridin-3-yl)ethan-1-amine (31 mg, 0.25 mmole) and the reaction was stirred overnight. NaBH4 (9.5 mg, 0.25 mmole) added, stir 10 minutes, 2 drops MeOH added, stir 1 h, quenched with water, organics separated off and evaporated. The residue was passed through a Gilson reverse phase HPLC to give {2-[(9R)-9-(pyridin-2-yl)-6-oxaspiro[4.5]decan-9-yl]ethyl}[2-(pyridin-3-yl)ethyl]amine, 65.3 mg (71%). LCMS m/z 367.1 (M+1) observed.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09044469B2
Quelldatensatzuspto-grants-2015_06
ORD IDord-ba46ae1e1bc44a82bc4fbf714ade0770
Quellennotizuspto-grants-2015_06