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HRID 131457作成日:2026年10月27日

(S)-2-(2-Methoxyethyl)piperazine → (S)-7-Chloro-10-[3-(2-methoxy-ethyl)-piperazin-1-yl]-2-methyl-4H-3-thia-4,9-diaza-benzo[f]azulene

https://huagongshe.com/reaction/131457

反応式

関与物質

役割名称HCID仕込み量
反応物(S)-2-(2-Methoxyethyl)piperazineHCID 55287560—
反応物7-chloro-2-methyl-4H-3-thia-4,9-diaza-benzo[f]azulen-10-ylamine hydrochlorideHCID 136388572—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
溶媒Dimethylsulfoxide tolueneHCID 22340214—
生成物(S)-7-Chloro-10-[3-(2-methoxy-ethyl)-piperazin-1-yl]-2-methyl-4H-3-thia-4,9-diaza-benzo[f]azuleneHCID 13609036160%

反応条件

温度130 °C

反応手順

Dissolve 7-chloro-2-methyl-4H-3-thia-4,9-diaza-benzo[f]azulen-10-ylamine hydrochloride (1.46 g, 4.86 mmol) and (S)-2-(2-methoxy-ethyl)-piperazine (2.1 g, 14.6 mmol) in dimethylsulfoxide/toluene (1:2)(18 ml), stir under nitrogen and heat in an oil bath at 130° C. for 28.5 hours. Stir 16 hours at ambient temperature. Dilute the mixture with water and ethyl acetate, and extract with ethyl acetate. Combine the ethyl acetate extracts, wash with water and brine, dry the organic phase (Na2SO4), filter and concentrate under reduced pressure. Chromatograph on silica gel (eluent: 0-10% 2N ammonia in methanol/dichloromethane) to give the title compound (1.14 g, 60%), Mass Spectrum (ESMS) 391/393 (M+1), mp 179-183° C. (dec).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07384934B2
出典データセットuspto-grants-2008_06
ORD IDord-0de79bc9bdcf4decb9130433baa099b5
出典メモuspto-grants-2008_06