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HRID 1186458Erstellt: 25. Oktober 2026

2-Bromo-1,1-dimethoxyethane → 8-Chloroimidazo[1,2-a]pyrazine

https://huagongshe.com/reaction/1186458

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Bromo-1,1-dimethoxyethaneHCID 81672—
Edukt2-Amino-3-chloropyrazineHCID 276224—
Edukt3-Bromo-8-chloroimidazo[1,2-a]pyrazineHCID 10059849—
Produkt8-Chloroimidazo[1,2-a]pyrazineHCID 10261286—

Reaktionsschritte

The starting materials are either commercially available or can be synthesized by methods known in the art. Compounds of formula Ia where X is N can be synthesized starting from the known 3-bromo-8-chloro-imidazo[1,2-a]pyrazine (4). Lumma, Jr., W. C.; Randall, W. C.; Cresson, E. L.; Huff, J. R.; Hartman, R. D.; Lyon, T. F. J. Med. Chem. 1983, 26, 357-363. Meurer, L. C.; Tolman, R. L.; Chapin, E. W.; Saperstein, R.; Vicario, P. P.; Zrada, M. M.; MacCoss, M. J. Med. Chem. 1992, 35, 3845-3857. In accordance to Scheme 1 below, 2-amino-3-chloropyrazine (1) can be reacted with 2-bromo-1,1-dimethoxy-ethane (2) to give 8-chloro-imidazo[1,2-a]pyrazine (3) which can be brominated to give 3-bromo-8-chloro-imidazo[1,2-a]pyrazine (4). Compound 4 can be reacted with an appropriate amine (HNR1R2) either in excess or in the presence of another base, such as diisopropyl ethyl amine, in an appropriate solvent, such as ethanol or butanol, between room temperature to reflux to give compound 5. Compound 5 can than be condensed with 2-methylsulfanyl-4-tributylstannanyl-pyrimidine (6) in the presence of a suitable palladium catalyst to give intermediate 7.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08673905B2
Quelldatensatzuspto-grants-2014_03
ORD IDord-f4274a20e8bb49af97cb15233eb2c9bd
Quellennotizuspto-grants-2014_03