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HRID 1005894作成日:2026年10月25日

5-(4-Chlorophenyl)-2-piperidin-4-ylpyrimidine → 4-(R)-Benzyl-3-(2-(R)-{4-[5-(4-chlorophenyl)pyrimidin-2-yl]piperidine-1-sulfonylmethyl}-3-methylbutyryl)oxazolidin-2-one

https://huagongshe.com/reaction/1005894

反応式

関与物質

役割名称HCID仕込み量
反応物5-(4-Chlorophenyl)-2-piperidin-4-ylpyrimidineHCID 22646697—
反応物4-(R)-benzyl-3-(2-(R)-chlorosulfonylmethyl-3 methylbutyryl)oxazolidin-2-oneHCID 22888284—
生成物4-(R)-Benzyl-3-(2-(R)-{4-[5-(4-chlorophenyl)pyrimidin-2-yl]piperidine-1-sulfonylmethyl}-3-methylbutyryl)oxazolidin-2-oneHCID 23519751100.1%

反応手順

Prepared according to the method for the preparation of 4-(R)-benzyl-3-(2-(R)-{4-[5-(4-fluorophenyl)pyrimidin-2-yl]piperazine-1-ulfonylmethyl}-3-methyl-butyryl)oxazolidin-2-one, from 5-(4-chlorophenyl)-2-piperidin-4-ylpyrimidine (0.123 g) and 4-(R)-benzyl-3-(2-(R)-chlorosulfonylmethyl-3-methylbutyryl)-oxazolidin-2-one (0.269 g), to yield the title compound as a cream foam (0.275 g, 100%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06787536B2
出典データセットuspto-grants-2004_09
ORD IDord-82a5310146cf4a298a87bad408ec975d
出典メモuspto-grants-2004_09