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HRID 521580作成日:2026年10月27日

Potassium Carbonate → 1-{3-Methyl-[1,2,4]triazolo[4,3-b]pyridazin-6-yl}-2-phenylpyrrolidine

https://huagongshe.com/reaction/521580

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2-PhenylpyrrolidineHCID 261892—
反応物6-Chloro-3-methyl-(1,2,4)triazolo(4,3-b)pyridazineHCID 911387—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物1-{3-Methyl-[1,2,4]triazolo[4,3-b]pyridazin-6-yl}-2-phenylpyrrolidineHCID 7111597012%

反応条件

温度100 °C

反応手順

A mixture of 6-chloro-3-methyl-[1,2,4]triazolo[4,3-b]pyridazine (200 mg, 1.19 mol), 2-phenylpyrrolidine (200 mg, 1.36 mmol) and K2CO3 (350 mg, 2.5 mmol) in acetonitrile (20 mL) was heated at 100° C. under microwave and stirred for 30 mins. After cooled to room temperature, the reaction mixture was diluted with water (20 mL) and extracted with ethyl acetate (20 mL*3). The combined organic layer was washed with brine (10 mL), dried over Na2SO4 and concentrated in vacuum. The residue was purified by prep-TLC (silica-gel, DCM: MeOH=20:1) to give product 3-methyl-6-(2-phenylpyrrolidin-1-yl)-[1,2,4]triazolo[4,3-b]pyridazine (Compound 10) as a white solid (30 mg, 12%). 1H NMR (300 MHz, CD3OD) δ 7.73-7.77 (d, 1H, J=10.2 Hz), 7.22-7.34 (m, 5H), 6.84-6.87 (d, 1H, J=10.2 Hz), 5.14-5.18 (m, 1H), 3.92-3.98 (m, 1H), 3.71-3.81 (m, 1H), 2.57 (s, 3H), 2.50-2.54 (M, 1H), 2.03-2.13 (m, 3H); LRMS (M+H+) m/z: calcd 279.15; found 279.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09328117B2
出典データセットuspto-grants-2016_05
ORD IDord-7c0bd7895aef4edd89798b32bf58533f
出典メモuspto-grants-2016_05