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HRID 251072作成日:2026年10月23日

Potassium Carbonate → (3,5-Dimethyl-pyridin-2-ylmethyl)-(4-pyrrolidin-1-yl-butyl)-amine

https://huagongshe.com/ja/reaction/251072

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物4-(Pyrrolidin-1-yl)butan-1-amineHCID 2762762—
反応物Sodium borohydrideHCID 4311764—
反応物3,5-Dimethylpyridine-2-carbaldehydeHCID 18731683—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物(3,5-Dimethyl-pyridin-2-ylmethyl)-(4-pyrrolidin-1-yl-butyl)-amineHCID 6727173633.1%

反応条件

温度0 °C

反応手順

A mixture of 4-pyrrolidin-1-yl-butylamine (0.180 g, 1.27 mmol) (Seguin, H. et al. Synth. Commun. 1998, 28, 4257-4272), 3,5-dimethyl-pyridine-2-carbaldehyde (0.171 g, 1.27 mmol) and K2CO3 (0.175 g, 1.27) in MeOH (5 mL) was stirred for 20 h. The mixture was filtered through a celite cake and the filtrate was cooled at 0° C. NaBH4 (0.048 g, 1.3 mmol) was added to the filtrate, and the mixture was stirred at for 1 h. Water (20 mL) was added and MeOH was removed. The aqueous residue was extracted with CH2Cl2 (3×20 mL). The organic extracts were combined and dried over anhydrous Na2SO4. After filtration the solvent was removed by evaporation under vacuum, and the residue was purified by flash chromatography on a silica gel column (100:5:3 CH2Cl2/MeOH/NH4OH), affording (3,5-dimethyl-pyridin-2-ylmethyl)-(4-pyrrolidin-1-yl-butyl)-amine as a colorless oil (0.110 g, 33%). 1H NMR (CDCl3) δ 1.54-1.58 (m, 4H), 1.72-1.76 (m, 4H), 2.24 (s, 3H), 2.25 (s, 3H), 2.39-2.46 (m, 6H), 2.66-2.71 (m, 2H), 3.81 (s, 2H), 7.21 (s, 1H), 8.18 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07863293B2
出典データセットuspto-grants-2011_01
ORD IDord-1b4077db23e34f339936f9716915d655
出典メモuspto-grants-2011_01