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HRID 1710383作成日:2026年10月25日

N,N-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene-1-sulfonamide → HCID 178486133、化合物

https://huagongshe.com/reaction/1710383

反応式

関与物質

役割名称HCID仕込み量
反応物N,N-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene-1-sulfonamideHCID 3868489—
反応物HCID 178516005HCID 178516005—
反応物HCID 178516006HCID 178516006—
溶媒Sodium CarbonateHCID 10340—
生成物HCID 178486133HCID 178486133—

反応手順

The title compound is analogously synthesized as described for 7-[2-(6-phenyl-3H-imidazo[4,5-b]pyridin-2-yl)-ethyl]-azepan-2-one (compound B1) from 100 mg of 7-[2-(6-bromo-3H-imidazo[4,5-b]pyridin-2-yl)-ethyl]-azepan-2-one (compound C1), 890 μl of aqueous sodium carbonate solution (strength 2.0 M), 138 mg N,N-dimethyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzenesulfonamide (compound C2), and 26 mg of trans-dichloro-bis(tricyclohexyl-phosphine)-palladium(II) at 160° C. for 30 min (microwave irradiation, power ≦300 W). Purification by chromatography on flash silica gel (eluent gradient: dichloromethane/0-10 vol. % ethanol) yields 93 mg of the title compound as a waxy solid. ESI-MS: 442.4 (MH+). TLC: Rf=0.41 (dichloromethane/ethanol 10:1 parts by volume).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07790710B2
出典データセットuspto-grants-2010_09
ORD IDord-2954c351b5b34ed2827228a25b0cc440
出典メモuspto-grants-2010_09