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HRID 52058作成日:2026年10月26日

Triethylamine → N-[4-(4-piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]pyrazole-4-carboxamide

https://huagongshe.com/reaction/52058

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Diethyl cyanophosphonateHCID 76257—
反応物Pyrazole-4-carboxylic acidHCID 3015937—
反応物2-Buten-1-amine, 4-[[4-(1-piperidinylmethyl)-2-pyridinyl]oxy]-, (Z)-HCID 13672473—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物N-[4-(4-piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]pyrazole-4-carboxamideHCID 4421124951%

反応手順

A solution of 2.39 g of 4-(4-piperidinomethyl-2-pyridyloxy) -cis-2-butenylamine and 1.08 g of 4-pyrazolecarboxylic acid in 40 ml of dry dimethylformamide was stirred for 5 minutes, whilst ice-cooling. 1.89 g of diethyl cyanophosphonate and 1.65 ml of triethylamine were added to the mixture, and the resulting mixture was stirred at room temperature for 3 hours. At the end of this time, the reaction mixture was diluted with water and extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium hydrogencarbonate and then with a saturated aqueous solution of sodium chloride, after which it was dried over anhydrous magnesium sulfate. The solvent was then removed by distillation under reduced pressure, and the residue was purified by column chromatography through silica gel, using a 1:9 by volume mixture of methanol and chloroform as the eluent, to give 1.65 g (yield 51%) of the title compound as a white powder, melting at 121°-123° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05616579
出典データセットuspto-grants-1997_04
ORD IDord-33e63b4db34046c6858d778f8790077d
出典メモuspto-grants-1997_04