With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.184950-35-4,(Tetrahydrofuran-3-yl)methanamine hydrochloride,as a common compound, the synthetic route is as follows.
5 – [(2,2,2-trifluoroethyl) oxymethyl] isoxazole-3-carboxylic acid (0.30 g, 1.3 mmol), Tetrahydrofuran-3-ylmethylamine hydrochloride (0.22 g, 1.6 mmol), Triethylamine (0.16 g, 1.6 mmol) And 1-hydroxybenzotriazole (0.02 g, 0.16 mmol) Was added to chloroform (amylene added product) (4 mL). To the mixture, 1-Ethyl-3- (3-dimethylaminopropyl) carbodiimide hydrochloride (0.31 g, 1.6 mmol) was added at room temperature, After stirring overnight, And concentrated under reduced pressure. Dilute hydrochloric acid was added to the concentrate, Extracted twice with ethyl acetate. The organic layer was washed with saturated brine, After drying with anhydrous sodium sulfate, And concentrated under reduced pressure. The residue was subjected to silica gel column chromatography, The following equationIndicated by N- (tetrahydrofuran-3-ylmethyl) -5 – [(2,2,2-trifluoroethyl) oxymethyl] isoxazole-3-carboxamide (Less than, This amide compound (128) is described. ) 0.32 g was obtained.
184950-35-4, 184950-35-4 (Tetrahydrofuran-3-yl)methanamine hydrochloride 17750392, aTetrahydrofurans compound, is more and more widely used in various fields.
Reference£º
Patent; SUMITOMO CHEMICAL COMPANY LIMITED; SUMITA, YUSUKE; (264 pag.)JP2015/51963; (2015); A;,
Tetrahydrofuran – Wikipedia
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