돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1184652생성일: 2026년 10월 25일

Dimethyl Sulfoxide → 7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-5-methylthiomethoxy-2,3,4,5-tetrahydro-1H-benzo[b]azepine

https://huagongshe.com/reaction/1184652

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물Acetic AnhydrideHCID 7918—
반응물Sodium HydroxideHCID 14798—
반응물TolvaptanHCID 216237—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
생성물7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-5-methylthiomethoxy-2,3,4,5-tetrahydro-1H-benzo[b]azepineHCID 25134215—

반응 조건

온도70 °C

반응 단계

Dimethylsulfoxide (DMSO) (3 ml), acetic anhydride (1.5 ml), and acetic acid (1.5 ml) were added to tolvaptan (1.0 g, 2.2 mmol), and the mixture was stirred at 70° C. for 4 hours. Water and 1N aqueous sodium hydroxide solution were added to the reaction mixture, and the mixture was extracted with ethyl acetate, washed with an aqueous saturated sodium chloride solution, dried over anhydrous sodium sulfate. After filtration and concentration under reduced pressure, the residue was purified by silica gel flash chromatography (n-hexane:ethyl acetate=80:20→20:80). The purified product was concentrated under reduced pressure to obtain 0.62 g of 7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-5-methylthiomethoxy-2,3,4,5-tetrahydro-1H-benzo[b]azepine as white amorphous solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08669229B2
출처 데이터셋uspto-grants-2014_03
ORD IDord-13aec5ad380546a894ea2d1be06e15f3
출처 메모uspto-grants-2014_03