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HRID 334112作成日:2026年10月25日

Methyl Methanesulfonate → 2,4-dichloro-5-methyl-5H-pyrrolo(3,2-d)pyrimidine

https://huagongshe.com/reaction/334112

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl MethanesulfonateHCID 4156—
反応物Cesium carbonateHCID 10796—
反応物2,4-Dichloro-5H-pyrrolo[3,2-d]pyrimidineHCID 5375053—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物2,4-dichloro-5-methyl-5H-pyrrolo(3,2-d)pyrimidineHCID 1472776387.1%

反応手順

A mixture of 2,4-dichloro-5H-pyrrolo[3,2-d]pyrimidine (2.67 g, 14.2 mmol), methanesulfonic acid methyl ester (1.26 mL, 14.9 mmol) and cesium carbonate (9.25 g, 28.4 mmol) in anhydrous N,N-dimethylformamide (21 mL) was stirred at RT (room temperature) under N2 for 15 h. The reaction mixture was diluted with ethyl acetate, and the organic layer was washed with 1:1 water/brine (3×) and brine (1×), dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography to give 2.50 g (87.1%) of 2,4-dichloro-5-methyl-5H-pyrrolo[3,2-d]pyrimidine as a white solid. MS(ESI) m/z: 202.2/204.1 [M+1]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08883799B2
出典データセットuspto-grants-2014_11
ORD IDord-ad4ab2b30ba54eb98fe767b36759613a
出典メモuspto-grants-2014_11