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HRID 69890作成日:2026年10月24日

1-Methyl-4-piperidone → 3-amino-6-bromo-N-(4-(3-(1-methylpiperidin-4-ylamino)piperidin-1-yl)pyridin-3-yl)pyrazine-2-carboxamide

https://huagongshe.com/ja/reaction/69890

反応式

関与物質

役割名称HCID仕込み量
反応物1-Methyl-4-piperidoneHCID 74049—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物3-amino-N-(4-(3-aminopiperidin-1-yl)pyridin-3-yl)-6-bromopyrazine-2-carboxamideHCID 86669178—
溶媒DichloromethaneHCID 6344—
生成物3-amino-6-bromo-N-(4-(3-(1-methylpiperidin-4-ylamino)piperidin-1-yl)pyridin-3-yl)pyrazine-2-carboxamideHCID 8666918866%

反応手順

To a solution of 3-amino-N-(4-(3-aminopiperidin-1-yl)pyridin-3-yl)-6-bromopyrazine-2-carboxamide in CH2Cl2 at room temperature was added 1-methylpiperidin-4-one (1.5 eq) followed by sodium triacetoxyborohydride (5.0 eq). The reaction was stirred at room temperature for 12 hours, concentrated, purified by reverse phase HPLC and lyophilized to provide 3-amino-6-bromo-N-(4-(3-(1-methylpiperidin-4-ylamino)piperidin-1-yl)pyridin-3-yl)pyrazine-2-carboxamide, (66%). LCMS (m/z): 489.2 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822497B2
出典データセットuspto-grants-2014_09
ORD IDord-a9fea1ac95f241c4858ab8725b7ddc2b
出典メモuspto-grants-2014_09