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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52091생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/52091

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Diethyl cyanophosphonateHCID 76257—
반응물Pyrazole-4-carboxylic acidHCID 3015937—
반응물3-({4-[(Piperidin-1-yl)methyl]pyridin-2-yl}oxy)propan-1-amineHCID 14625102—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물N-[3-(4-Piperidinomethyl-2-pyridyloxy)propyl]-pyrazole-4-carboxamideHCID 1996287987.1%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616579
출처 데이터셋uspto-grants-1997_04
ORD IDord-85d42b925841424baebdad4bc27153ca
출처 메모uspto-grants-1997_04