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HRID 40525作成日:2026年10月25日

Cesium carbonate → (S)-N-(1-{4-[3-(2,3-Difluoro-4-methyl-phenoxy)-azetidin-1-yl]-phenyl}-ethyl)-acetamide

https://huagongshe.com/reaction/40525

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Methanesulfonyl chlorideHCID 31297—
反応物2,3-Difluoro-4-methylphenolHCID 2774151—
反応物(S)-N-{1-[4-(3-Hydroxy-azetidin-1-yl)-phenyl]ethyl}-acetamideHCID 86689005—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒DimethylacetamideHCID 31374—
生成物(S)-N-(1-{4-[3-(2,3-Difluoro-4-methyl-phenoxy)-azetidin-1-yl]-phenyl}-ethyl)-acetamideHCID 86689026—

反応条件

温度0 °C

反応手順

To 0.023 g (0.10 mmol) (S)—N-{1-[4-(3-hydroxy-azetidin-1-yl)-phenyl]-ethyl}-acetamide (V.1) in 5 mL THF are added 0.017 mL (0.12 mmol) TEA and the mixture is cooled to 0° C. 0.008 mL (0.10 mmol) methanesulfonyl chloride are added dropwise and the mixture is stirred for 2 h at 0° C. Water is added and the aq. phase is extracted with ethyl acetate (2×). The combined organic layers are dried (MgSO4) and concentrated. The residue is taken up in 1.0 mL DMA and is added to a mixture of 0.014 g (0.12 mmol) 2,3-difluoro-4-methylphenol and 0.039 g (0.12 mmol) Cs2CO3 in 1.0 mL DMA. The resulting mixture is stirred for 12 h at 100° C. After cooling the mixture is directly purified by HPLC (MeOH/water (+0.1% NH4OH)) to yield the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530461B2
出典データセットuspto-grants-2013_09
ORD IDord-61c7ced06ea8445ebbf1b886e10cbb3f
出典メモuspto-grants-2013_09