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HRID 1887890作成日:2026年10月25日

4-Methanesulfonylpiperidine hydrochloride → 4-Methanesulfonyl-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-5'-carboxylic acid (7-chloro-4-oxo-1-phenyl-1,4-dihydro-quinolin-3-ylmethyl)-amide

https://huagongshe.com/reaction/1887890

反応式

関与物質

役割名称HCID仕込み量
反応物4-Methanesulfonylpiperidine hydrochlorideHCID 23061698—
反応物6-chloro-N-((7-chloro-4-oxo-1-phenyl-1,4-dihydroquinolin-3-yl)methyl)nicotinamideHCID 71487063—
生成物4-Methanesulfonyl-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-5'-carboxylic acid (7-chloro-4-oxo-1-phenyl-1,4-dihydro-quinolin-3-ylmethyl)-amideHCID 71217358—

反応手順

4-Methanesulfonyl-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-5′-carboxylic acid (7-chloro-4-oxo-1-phenyl-1,4-dihydro-quinolin-3-ylmethyl)-amide was prepared starting from intermediate E and 4-methanesulfonyl piperidine hydrochloride. MS calcd. for C28H27ClN4O4S [(M+H)+] 551.1, obsd. 551.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08501732B2
出典データセットuspto-grants-2013_08
ORD IDord-7460c91f1ff9410d9dea8cd318fbc888
出典メモuspto-grants-2013_08