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HRID 1649478作成日:2026年10月27日

Cyanoacetamide → Milrinone

https://huagongshe.com/reaction/1649478

反応式

関与物質

役割名称HCID仕込み量
反応物CyanoacetamideHCID 7898—
反応物4-Ethoxy-3-(4-pyridyl)-3-buten-2-oneHCID 3021227—
反応物Sodium MethoxideHCID 10942334—
生成物MilrinoneHCID 4197—

反応手順

In another of its aspects the invention resides in the process which comprises reacting 2-(lower-alkoxy)-1-(pyridinyl)ethenyl lower-alkyl ketone of formula II with cyanoacetamide or malonamide in the presence of a condensing agent and neutralizing the reaction mixture to produce 1,2-dihydro-6-R-2-oxo-5-PY-nicotinonitrile or 1,2-dihydro-6-R-2-oxo-5-PY-nicotinamide of formula III, where R, R', PY and Q have the meanings given for formula III. In preferred embodiments 2-ethoxy(or methoxy)-1-(4- or 3-pyridinyl)ethenyl methyl(or ethyl) ketone is reacted with cyanoacetamide or malonamide in the presence of an alkali lower-alkoxide, preferably sodium methoxide, and then the reaction mixture is neutralized to produce 1,2-dihydro-6-methyl(or ethyl)-2-oxo-5-[4(or 3)-pyridinyl]nicotinonitrile or 1,2-dihydro-6-methyl(or ethyl)-2-oxo-5-[4(or 3)-pyridinyl]nicotinamide, respectively. In a particularly preferred embodiment 2-ethoxy-1-(4-pyridinyl)ethenyl methyl ketone is reacted with cyanoacetamide in the presence of sodium methoxide and the reaction mixture is neutralized to produce 1,2-dihydro-6-methyl-2-oxo-5-(4 -pyridinyl)nicotinonitrile.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04417054
出典データセットuspto-grants-1983_11
ORD IDord-454b4500ba17423fa7ee3bccaca04310
出典メモuspto-grants-1983_11