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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52058생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/52058

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Diethyl cyanophosphonateHCID 76257—
반응물Pyrazole-4-carboxylic acidHCID 3015937—
반응물2-Buten-1-amine, 4-[[4-(1-piperidinylmethyl)-2-pyridinyl]oxy]-, (Z)-HCID 13672473—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물N-[4-(4-piperidinomethyl-2-pyridyloxy)-cis-2-butenyl]pyrazole-4-carboxamideHCID 4421124951%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616579
출처 데이터셋uspto-grants-1997_04
ORD IDord-33e63b4db34046c6858d778f8790077d
출처 메모uspto-grants-1997_04