반응 #44417

반응 방정식

(1S)-1,2,3,4-tetrahydronaphthalen-1-amine

1-(6-chloropyrazin-2-yl)-1H-benzimidazole-5-carbonitrile

1-(6-chloropyrazin-2-yl)-1H-benzimidazole-6-carbonitrile

→

1-{6[(1S)-1,2,3,4-tetrahydronaphthalen-1-ylamino]pyrazin-2-yl}-1H-benzimidazole-6-carbonitrile

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후처리

1. 1
   기타The product was obtained as a mixture of regioisomers which
2. 2
   기타were separated by column chromatography

실험 절차

In an analogous fashion to Example 1, an approximately 1:1 mixture of 1-(6-chloropyrazin-2-yl)-1H-benzimidazole-5-carbonitrile and 1-(6-chloropyrazin-2-yl)-1H-benzimidazole-6-carbonitrile (100 mg, 0.39 mmol) was condensed with (1S)-1,2,3,4-tetrahydronaphthalen-1-amine (69 mg, 0.47 mmol). The product was obtained as a mixture of regioisomers which were separated by column chromatography using dichloromethane-methanol (95:5) as eluant. From the less polar fractions 1-{6[(1S)-1,2,3,4-tetrahydronaphthalen-1-ylamino]pyrazin-2-yl}-1H-benzimidazole-6-carbonitrile was obtained as a yellow semi-solid (26 mg).

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