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HRID 474130作成日:2026年10月26日

Cesium carbonate → 6-Chloro-1-(2,2-difluoro-ethyl)-1H-pyrrolo[3,2-b]pyridine-5-carboxylic acid ethyl ester

https://huagongshe.com/reaction/474130

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物Ammonium ChlorideHCID 25517—
反応物1,1-Difluoro-2-iodoethaneHCID 3833565—
反応物Ethyl 6-chloro-1H-pyrrolo[3,2-B]pyridine-5-carboxylateHCID 60058581—
触媒Tetrabutylammonium IodideHCID 67553—
溶媒DimethylformamideHCID 6228—
生成物6-Chloro-1-(2,2-difluoro-ethyl)-1H-pyrrolo[3,2-b]pyridine-5-carboxylic acid ethyl esterHCID 68108563—

反応手順

To a solution of 6-chloro-1H-pyrrolo[3,2-b]pyridine-5-carboxylic acid ethyl ester (210 mg, 0.935 mmol) in DMF (10 ml) was added cesium carbonate (457 mg, 1.402 mmol), after 15 min stirring at room temperature 1,1-difluoro-2-iodoethane (538 mg, 2.8 mmol) was added and stirring was continued over night. Tetrabutylammonium iodide (34.5 mg, 0.093 mmol) was added and stirring was continued for another 48 h. To the reaction mixture was added saturated aq. NH4Cl and the mixture was extracted with MTBE (2×). The combined organic layers were washed with half-saturated aq. NaCl, dried with Na2SO4 and evaporated. The residue was purified by chromatography on silica gel (cyclohexane to cyclohexane/EtOAc 20:80) to provide the title compound as yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08637508B2
出典データセットuspto-grants-2014_01
ORD IDord-7b1797d9289b4b31b92ec45e3274229f
出典メモuspto-grants-2014_01