首页> 外国专利> SYNTHESIS OF ORTHOHALOGENATED PYRIDINE CARBOXYLIC ACID PYRIDINE CARBOXYLIC ACID AMIDE AND NEW ORTHOHALOGENATED PYRIDINE CARBOXYLIC ACID OR PYRIDINE CARBOXYLIC ACID AMIDE

SYNTHESIS OF ORTHOHALOGENATED PYRIDINE CARBOXYLIC ACID PYRIDINE CARBOXYLIC ACID AMIDE AND NEW ORTHOHALOGENATED PYRIDINE CARBOXYLIC ACID OR PYRIDINE CARBOXYLIC ACID AMIDE

机译:邻苯二甲酰化吡啶羧酸羧酸和新的邻苯二甲酰化吡啶羧酸羧酸或吡啶羧酸酰胺的合成

摘要

PURPOSE: To synthesize orthohalogenated pyridine carboxylic acid or pyridine carboxylic acid amide that is important as a synthetic intermediate of medical products or plant disinfectants. ;CONSTITUTION: Orthohalogenated pyridine carboxylic acid is obtained by reacting hologenated pyridine with organic lithium derivative and then with carbon dioxide and subsequently by acidifying the reacting solution after hydrolysis. Organic lithium derivative is selected from the group consisting of alkyl- lithium, aryl-lithium, or N,N-2 substituted aliphatic lithium amide. X-carboxy or carboxyamide-(X+1)-fluoropyridine (X is 2 or 3), 3-carboxy or carboxyamide-4-trifluoromethyl-2-halo genopyridine, 3-carboxy or carboxyamide-2,4-dihalogenopyridine are new compounds.;COPYRIGHT: (C)1993,JPO
机译:用途:合成对医疗产品或植物消毒剂的合成中间体很重要的邻卤代吡啶羧酸或吡啶羧酸酰胺。 ;组成:原卤代吡啶羧酸是通过使卤代吡啶与有机锂衍生物反应,然后与二氧化碳反应,然后在水解后酸化反应溶液而获得的。有机锂衍生物选自烷基-锂,芳基-锂或N,N-2取代的脂族锂酰胺。 X-羧基或羧酰胺-(X + 1)-氟吡啶(X为2或3),3-羧基或羧酰胺-4-三氟甲基-2-卤代庚啶,3-羧基或羧酰胺-2,4-二卤代吡啶。;版权:(C)1993,日本特许厅

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