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HRID 52091作成日:2026年10月25日

Triethylamine → N-[3-(4-Piperidinomethyl-2-pyridyloxy)propyl]-pyrazole-4-carboxamide

https://huagongshe.com/reaction/52091

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3-({4-[(Piperidin-1-yl)methyl]pyridin-2-yl}oxy)propan-1-amineHCID 14625102—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物N-[3-(4-Piperidinomethyl-2-pyridyloxy)propyl]-pyrazole-4-carboxamideHCID 1996287987.1%

反応手順

A solution of 1.0 g of 3-(4-piperidinomethyl-2-pyridyloxy)propylamine and 0.45 g of 4-pyrazolecarboxylic acid dissolved in 15 ml of dimethylformamide was stirred for 5 minutes, whilst ice-cooling, after which 734 mg of diethyl cyanophosphonate and 0.68 ml of triethylamine were added to the resulting mixture. The mixture was then stirred at room temperature for 3 hours, after which it was diluted with water, and the aqueous mixture was 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, and dried over anhydrous magnesium sulfate. The solvent was then removed by distillation under reduced pressure, and the resulting 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 1.2 g (yield 85%) of the title compound as a white powder, melting at 117°-119° 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-85d42b925841424baebdad4bc27153ca
出典メモuspto-grants-1997_04