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HRID 1978981作成日:2026年10月25日

3-Pyridinecarboxylic acid, 4-(trifluoromethyl)- → Tert-butyl 3-amino-3-(4-trifluoromethyl-3-pyridinecarbonyloxyimino)propionate

https://huagongshe.com/reaction/1978981

反応式

関与物質

役割名称HCID仕込み量
反応物3-Pyridinecarboxylic acid, 4-(trifluoromethyl)-HCID 2777549—
反応物Bis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
反応物tert-butyl 2-(N'-hydroxycarbamimidoyl)acetateHCID 76589802—
溶媒TetrahydrofuranHCID 8028—
生成物Tert-butyl 3-amino-3-(4-trifluoromethyl-3-pyridinecarbonyloxyimino)propionateHCID 5393129951.6%

反応手順

30 g of 4-trifluoromethyl-3-pyridinecarboxylic acid is initially charged in 150 ml of dry THF and, a little at a time, admixed with 25.3 g of carbonyl-diimidazole. The mixture is stirred at room temperature for 30 min. 27.2 g of tert-butoxycarbonylacetamide oxime dissolved in 150 ml of THF are then added dropwise. The mixture is stirred overnight, the solvent is evaporated and the residue is taken up in ethyl acetate, washed three times with 1 M sulfuric acid and once with saturated sodium bicarbonate solution. Concentration of the ethyl acetate phase gives 28 g of the product as a pale yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06239160B1
出典データセットuspto-grants-2001_05
ORD IDord-fdaa577ba9fd42aa8988ed42e6d7917c
出典メモuspto-grants-2001_05