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HRID 443793作成日:2026年10月26日

Pyridine → 1-methyl-7-chloro-3-dipropylacetoxy-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepine-2-one

https://huagongshe.com/reaction/443793

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物TemazepamHCID 5391—
反応物2-Propylvaleryl chlorideHCID 76240—
溶媒DimethylformamideHCID 6228—
生成物1-methyl-7-chloro-3-dipropylacetoxy-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepine-2-oneHCID 23465564—

反応手順

A solution of 15 g of 1-methyl-7-chloro-3-hydroxy-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepine-2-one (Temazepam) and 5 g of absolute pyridine is cooled in 40 ml of freshly distilled dimethyl formamide to -5° and is mixed drop by drop with 10.5 g of dipropyl acetic acid chloride with the exclusion of atmospheric moisture. The mixture is stirred for an additional 4 hours at -5° and is allowed to stand over night at 0°, and then the mixture is poured on ice. The separated oil crystallizes while rubbed on with ethanol. By recrystallization from petroleum ether or isopropanol using activated charcoal, one will obtain the 1-methyl-7-chloro-3-dipropylacetoxy-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepine-2-one as a colorless powder with a melting point of 134°-136°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04261987
出典データセットuspto-grants-1981_04
ORD IDord-b58383cd293c40228718e3d99a150283
出典メモuspto-grants-1981_04