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HRID 223358생성일: 2026년 10월 26일

Sulmazole → 2-(2-Methoxy-4-methylsulfinyl-phenyl)-6-hydroxy-1H-imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/223358

반응식

참여 물질

역할이름HCID투입량
반응물SulmazoleHCID 5353—
반응물Ethylenediaminetetraacetic AcidHCID 6049—
반응물L-Ascorbic AcidHCID 54670067—
촉매Ferrous SulfateHCID 24393—
용매Hydrogen PeroxideHCID 784—
용매PhosphateHCID 1061—
생성물2-(2-Methoxy-4-methylsulfinyl-phenyl)-6-hydroxy-1H-imidazo[4,5-b]pyridineHCID 13036815—

반응 단계

7.2 gm of 2-(2-methoxy-4-methylsulfinyl-phenyl)-1H-imidazo[4,5-b]pyridine were dissolved in a mixture of a phosphate buffer of pH 7.2 and 120 ml of 3% hydrogen peroxide, and a solution of 9.3 gm of ethylenediamine tetraacetic acid, 4.4 gm of ascorbic acid, 3.8 gm of iron(II) sulfate in a phosphate buffer of pH 7.2 was added. After 30 minutes the reaction mixture was evaporated in vacuo, and the residue was purified by chromatography on a polystyrene resin column (XAD-2 of Rohm & Haas) with water and methanol as eluants. After evaporation of the eluate the two compounds were separated by means of chromatography on silicagel [eluant: chloroform/methanol/ammonia water=85/15/2 (v/v)]. 2-(2-Methoxy-4-methylsulfinyl-phenyl)-6-hydroxy-1H-imidazo[4,5-b]pyridine was obtained as yellow powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04353909
출처 데이터셋uspto-grants-1982_10
ORD IDord-82029858ee1c4b3dbc75f90598e80ee4
출처 메모uspto-grants-1982_10