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HRID 485393作成日:2026年10月26日

Thionyl Chloride → 1,3-dimethyl-N-[4-[3-(1-piperidinylmethyl)phenoxy]butyl]-1H-1,2,4-triazole-5-amine

https://huagongshe.com/reaction/485393

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物1,3-dimethyl-1H-1,2,4-triazol-5-amineHCID 307975—
反応物4-[3-(1-Piperidinylmethyl)phenoxy]butanoic acidHCID 14221805—
反応物Aluminium lithium hydrideHCID 21226445—
触媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物1,3-dimethyl-N-[4-[3-(1-piperidinylmethyl)phenoxy]butyl]-1H-1,2,4-triazole-5-amineHCID 2027029333.1%

反応手順

A stirred suspension of 4-[3-(1-piperidinylmethyl)phenoxy]butanoic acid (4.0 g) in methylene chloride (100 ml) and dimethylformamide (24 drops) was treated with thionyl chloride (5.16 g). The solution was stirred at room temperature for 18 h and evaporated in vacuo, to give a pale yellow solid which was dissolved in methylene chloride (100 ml) and treated with 5-amino-1,3-dimethyl-1,2,4-triazole (1.61 g). The reaction mixture was stirred at room temperature for 24 h and evaporated in vacuo. The residue was dissolved in aqueous sodium bicarbonate solution and extracted with ethyl acetate. The organic extracts were dried and evaporated to give a brown oil which was dissolved in tetrahydrofuran (500 ml), treated with lithium aluminium hydride (3.04 g), stirred at room temperature for 18 h and refluxed for 3 h. The cooled reaction mixture was quenched with water (300 ml) and extracted with ethyl acetate. The combined extracts were washed with brine, dried and evaporated in vacuo to give an oil which was distilled to give the title compound (1.7 g) as a pale yellow oil, b.p. 230°/0.06 mm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04536508
出典データセットuspto-grants-1985_08
ORD IDord-6d7c22e4360d49bba0b2e04a07a185e1
出典メモuspto-grants-1985_08