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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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2-Bromo-1,1-dimethoxyethane | HCID 81672 | — |
| Edukt | 2-Amino-3-chloropyrazine | HCID 276224 | — |
| Edukt | 3-Bromo-8-chloroimidazo[1,2-a]pyrazine | HCID 10059849 | — |
| Produkt | 8-Chloroimidazo[1,2-a]pyrazine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08673905B2 |
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| Quelldatensatz | uspto-grants-2014_03 |
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| ORD ID | ord-f4274a20e8bb49af97cb15233eb2c9bd |
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| Quellennotiz | uspto-grants-2014_03 |
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