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HRID 1730185作成日:2026年10月27日

N,N-Dimethyl-1,3-propanediamine → 2-[2-(3-Dimethylaminopropylamino)-5-thiadiazolyl]-1-methyl-5-nitroimidazole

https://huagongshe.com/reaction/1730185

反応式

関与物質

役割名称HCID仕込み量
反応物N,N-Dimethyl-1,3-propanediamineHCID 7993—
反応物Sodium BicarbonateHCID 516892—
反応物2-(2-Chloro-5-thiadiazolyl)-1-methyl-5-nitroimidazoleHCID 21390801—
溶媒BenzeneHCID 241—
生成物2-[2-(3-Dimethylaminopropylamino)-5-thiadiazolyl]-1-methyl-5-nitroimidazoleHCID 21390856—

反応手順

A mixture consisting of 3.8 gm., 0.0155 mole of 2-(2-chloro-5-thiadiazolyl)-1-methyl-5-nitroimidazole, prepared as in Example 16 2.5 gm., 0.029 mole of 3-dimethylaminopropylamine, 2.1 gm. 0.025 mole, of sodium bicarbonate and 100 ml. of benzene is refluxed for 22 hours. The reaction mixture is cooled to room temperature, washed with aqueous sodium bicarbonate and sodium chloride solutions. Cooling to 5° C. gives a crystalline precipitate which is collected and recrystallized from benzene to give the pure compound melting at 153°-154° C. More product is obtained from the mother liquors to give an overall yield of 3.0 gm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03991200
出典データセットuspto-grants-1976_11
ORD IDord-99b246c9bdc8479c9a0236635a3792a8
出典メモuspto-grants-1976_11