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HRID 551577作成日:2026年10月27日

Diethyl Ether → (4-Isopropyl-piperazin-1-yl)-(6-piperidin-1-ylmethyl-pyridin-3-yl)-methanone

https://huagongshe.com/reaction/551577

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物1-IsopropylpiperazineHCID 78013—
反応物Magnesium BromideHCID 82241—
反応物(4-Isopropyl-piperazin-1-yl)-(6-piperidin-1-ylmethyl-pyridin-3-yl)-methanoneHCID 11522780—
反応物Methyl 6-(piperidin-1-ylmethyl)nicotinateHCID 44515770—
溶媒TetrahydrofuranHCID 8028—
生成物AmmoniaHCID 2223%
生成物(4-Isopropyl-piperazin-1-yl)-(6-piperidin-1-ylmethyl-pyridin-3-yl)-methanoneHCID 1152278070%

反応手順

(4-Isopropyl-piperazin-1-yl)-(6-piperidin-1-ylmethyl-pyridin-3-yl)-methanone. A solution of 6-piperidin-1-ylmethyl-nicotinic acid methyl ester (0.300 g, 1.28 mmol), and MgBr2.OEt2 (0.900 g, 3.84 mmol) in THF (15 mL) was stirred for 15 min. A solution of 1-isopropyl-piperazine (0.325 g, 2.56 mmol) in THF (2 mL) was then added to the reaction drop-wise and the mixture was heated at reflux for 48 h. The reaction mixture was cooled to rt, concentrated, treated with 1 N aq. NaHCO3 (50 mL), and extracted with ethyl acetate (3×50 mL). The organic layers were combined, dried (Na2SO4), and concentrated. Chromatography of the residue (SiO2; 3-6% 2 M NH3 in MeOH/DCM) gave the title compound as an oil (0.297 g, 70%). MS (ESI): exact mass calcd. for C19H30N4O, 330.2; m/z found, 331.2 [M+H]+. 1H NMR (400 MHz, CDCl3): 8.55 (d, J=2.2, 1H), 7.87 (dd, J=7.8, 2.0, 1H), 7.62 (d, J=7.6, 1H), 3.78 (br s, 2H), 3.67 (s, 2H), 3.48 (br s, 2H), 2.77-2.73 (m, 1H), 2.65-2.48 (m, 8H), 1.65-1.59 (m, 4H), 1.49-1.48 (m, 2H), 1.09 (d, J=6.6, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07947718B2
出典データセットuspto-grants-2011_05
ORD IDord-f9382c9d72f0458aa7a95e165314612d
出典メモuspto-grants-2011_05