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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16826Erstellt: 26. Oktober 2026

Octahydropyrrolo(1,2-a)pyrazine → 5-(3,4,6,7,8,8a-Hexahydro-1H-pyrrolo[2,1-c]pyrazin-2-yl)-N-[5-[(3,5-dimethoxyphenyl)methoxy]-2H-pyrazol-3-yl]pyrazine-2-carboxamide

https://huagongshe.com/reaction/16826

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOctahydropyrrolo(1,2-a)pyrazineHCID 558578—
Edukt5-Chloro-N-[5-[(3,5-dimethoxyphenyl)methoxy]-2H-pyrazol-3-yl]pyrazine-2-carboxamideHCID 86621073—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt5-(3,4,6,7,8,8a-Hexahydro-1H-pyrrolo[2,1-c]pyrazin-2-yl)-N-[5-[(3,5-dimethoxyphenyl)methoxy]-2H-pyrazol-3-yl]pyrazine-2-carboxamideHCID 6658986237,4%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

5-Chloro-N-[5-[(3,5-dimethoxyphenyl)methoxy]-2H-pyrazol-3-yl]pyrazine-2-carboxamide (585 mg, 1.50 mmol) was added in one portion to 1,2,3,4,6,7,8,8a-octahydropyrrolo[1,2-a]pyrazine (379 mg, 3.00 mmol) in anhydrous dimethylsulfoxide (1.50 ml) at 25° C. The resulting solution was stirred at 100° C. for 18 h. The residue was purified by ion exchange chromatography, using an SCX column. The desired product was eluted from the column using 7M NH3/MeOH to afford impure material. The concentrated eluent was purified by preparative HPLC, using decreasingly polar mixtures of water (containing 1% NH3) and MeCN as eluents. Fractions containing the desired compound were evaporated to dryness to afford impure product as a yellow solid. The impure material was then repurified by silica column chromatography, eluting with a gradient of 0 to 5% 7M NH3/MeOH in DCM. Pure fractions were evaporated to dryness to afford the title compound (269 mg, 37%) as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737149B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-cbaed1bb1a61496bb30fc541ae73d34c
Quellennotizuspto-grants-2010_06