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HRID 1750460Erstellt: 26. Oktober 2026

Hydrochloric Acid → (1S,2S)-1-N-[5-(Trifluoromethyl)pyridin-2-yl]cyclopentane-1,2-diamine hydrochloride

https://huagongshe.com/reaction/1750460

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt1,4-DioxaneHCID 31275—
EduktDiisopropylethylamineHCID 81531—
Edukt2-Chloro-5-(trifluoromethyl)pyridineHCID 92342—
Edukt(1S,2S)-trans-N-Boc-1,2-cyclopentanediamineHCID 17040218—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelMethanolHCID 887—
Produkt(1S,2S)-1-N-[5-(Trifluoromethyl)pyridin-2-yl]cyclopentane-1,2-diamine hydrochlorideHCID 118308256—

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

A microwave vial was charged with tert-butyl N-[(1S,2S)-2-aminocyclopentyl]carbamate (CAS number 586961-34-4; 1.0 g, 4.99 mmol), 2-chloro-5-(trifluoromethyl)pyridine (CAS number 52334-81-3; 0.997 g, 5.49 mmol), DIPEA (2.62 ml, 14.98 mmol) and DMSO (16.6 ml). The reaction was heated with microwave irradiation at 140° C. for 2 hours and then partitioned between ethyl acetate and water. The organics were washed with water and brine, dried over magnesium sulfate, filtered and concentrated in vacuo. This was then purified by column chromatography (silica, 0-50% ethyl acetate/petrol) to afford a cream solid to which was then added methanol (10 ml) and HCl in 1,4-dioxane (4M, 6.24 ml, 24.97 mmol) and the reaction was stirred at room temperature for 17 hours. The reaction mixture was concentrated in vacuo and azeotropically distilled with toluene to afford the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09156829B2
Quelldatensatzuspto-grants-2015_10
ORD IDord-adfe6d8e595d40458419aeedf13db212
Quellennotizuspto-grants-2015_10