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HRID 23398作成日:2026年10月24日

5-chloro-1-(4,5-dihydro-1H-imidazol-2-ylmethyl)-3-[2-(tetrahydro-pyran-2-yloxy)-ethanesulfonyl]-1H-indole → 2-[5-Chloro-1-(4,5-dihydro-1H-imidazol-2-ylmethyl)-1H-indole-3-sulfonyl]-ethanol

https://huagongshe.com/ja/reaction/23398

反応式

関与物質

役割名称HCID仕込み量
反応物5-chloro-1-(4,5-dihydro-1H-imidazol-2-ylmethyl)-3-[2-(tetrahydro-pyran-2-yloxy)-ethanesulfonyl]-1H-indoleHCID 22573990—
溶媒Acetic acid--water (1/1)HCID 21899381—
生成物2-[5-Chloro-1-(4,5-dihydro-1H-imidazol-2-ylmethyl)-1H-indole-3-sulfonyl]-ethanolHCID 22574068—

反応条件

温度47.5 °C

反応手順

The 5-chloro-1-(4,5-dihydro-1H-imidazol-2-ylmethyl)-3-[2-(tetrahydro-pyran-2-yloxy)-ethanesulfonyl]-1H-indole (0.028 g) prepared in the previous Step was dissolved in 4 ml acetic acid:water (2:1) and stirred at 45-50° C. for 3 h. The solvents were removed under reduced pressure and the crude product was purified by column chromatography (silica gel) eluting with 3-5% methanol in methylene chloride with 0.1% ammonium hydroxide added. The 2-[5-Chloro-1-(4,5-dihydro-1H-imidazol-2-ylmethyl)-1H-indole-3-sulfonyl]-ethanol thus obtained weighed 0.005 g after drying.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06852726B2
出典データセットuspto-grants-2005_02
ORD IDord-99f5b152a87f44f1b7471a0d3254f0ff
出典メモuspto-grants-2005_02