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HRID 1024918作成日:2026年10月25日

4-chloro-2-[[(2,3-difluorophenyl)methyl]thio]-6-[(1R)-1-methyl-2-(triphenylmethoxy)ethoxy]-pyrimidine → 5-(azetidin-1-ylcarbonyl)-N-{2-[(2,3-difluorobenzyl)thio]-6-[(1R)-1-methyl-2-(triphenylmethyloxy)ethoxy]pyrimidin-4-yl}furan-2-sulfonamide

https://huagongshe.com/reaction/1024918

反応式

関与物質

役割名称HCID仕込み量
反応物4-chloro-2-[[(2,3-difluorophenyl)methyl]thio]-6-[(1R)-1-methyl-2-(triphenylmethoxy)ethoxy]-pyrimidineHCID 53628345—
反応物5-(Azetidin-1-ylcarbonyl)furan-2-sulfonamideHCID 53628365—
生成物5-(azetidin-1-ylcarbonyl)-N-{2-[(2,3-difluorobenzyl)thio]-6-[(1R)-1-methyl-2-(triphenylmethyloxy)ethoxy]pyrimidin-4-yl}furan-2-sulfonamideHCID 53628364—

反応手順

The subtitle compound was prepared from 5-(azetidin-1-ylcarbonyl)furan-2-sulfonamide (the product of step iii) (0.40 g) and 4-chloro-2-[[(2,3-difluorophenyl)methyl]thio]-6-[(1R)-1-methyl-2-(triphenylmethoxy)ethoxy]-pyrimidine (the product of Example 13, step iii) (0.41 g) according to the procedure outlined in Example 1, step iv). Yield: 0.25 g

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08722883B2
出典データセットuspto-grants-2014_05
ORD IDord-b3a1f26254704b0b8e84f0c5613af39d
出典メモuspto-grants-2014_05