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HRID 54965作成日:2026年10月25日

Sodium hydride → 3-[(4,5-Dihydro-4-methyl-1-phenyl-1H-2,4-benzodiazepin-3-yl)thio]-N,N-diethylpropaneamine

https://huagongshe.com/reaction/54965

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物3-Chloropropyl(diethyl)amineHCID 66918—
反応物Maleic AcidHCID 444266—
反応物1,2,4,5-Tetrahydro-4-methyl-1-phenyl-3H-2,4-benzodiazepin-3-thioneHCID 14978307—
溶媒AcetoneHCID 180—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物3-[(4,5-Dihydro-4-methyl-1-phenyl-1H-2,4-benzodiazepin-3-yl)thio]-N,N-diethylpropaneamineHCID 1995717376.9%

反応手順

A solution of of 12 g (45 mmol) of 1,2,4,5-tetrahydro-4-methyl-1-phenyl-3H-2,4-benzodiazepin-3-thione of Example 152 in 100 mL of DMF was treated with 1.24 g (50 mmol) of sodium hydride at 70° and 7.5 g (50 mmol) of 3-diethylaminopropyl chloride was added dropwise at 70°. The reaction was stirred at 70° for five hours and then at room temperature for two days. The reaction was poured into 250 mL of ice water and extracted twice into ethyl acetate. The product was extracted into 150 mL of 2N HCl, washed with ethyl acetate, made basic, and extracted back into ethyl acetate. The ethyl acetate solution was dried over magnesium sulfate, stripped, and the residue was dissolved in acetone. Two equivalents of maleic acid in 40 mL of acetone was added, followed by a small amount of ether. The resulting precipitate was recrystallized from acetone/ether to provide 13.2 g of product as the dimaleate salt, mp 95-97.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05624922
出典データセットuspto-grants-1997_04
ORD IDord-395a49f80d564bfdbdf21a568a86ba02
出典メモuspto-grants-1997_04