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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54965생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/54965

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물3-Chloropropyl(diethyl)amineHCID 66918—
반응물Maleic AcidHCID 444266—
반응물1,2,4,5-Tetrahydro-4-methyl-1-phenyl-3H-2,4-benzodiazepin-3-thioneHCID 14978307—
용매AcetoneHCID 180—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물3-[(4,5-Dihydro-4-methyl-1-phenyl-1H-2,4-benzodiazepin-3-yl)thio]-N,N-diethylpropaneamineHCID 1995717376.9%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624922
출처 데이터셋uspto-grants-1997_04
ORD IDord-395a49f80d564bfdbdf21a568a86ba02
출처 메모uspto-grants-1997_04