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HRID 1951096作成日:2026年10月25日

4-Fluorobenzoyl chloride → N-{(3RS,4SR)-4-(3,4-Dichloro-phenyl)-1-[1-(1-methyl-cyclopropanecarbonyl)-piperidine-4-carbonyl]-pyrrolidin-3-yl}-4-fluoro-N-methyl-benzamide

https://huagongshe.com/reaction/1951096

反応式

関与物質

役割名称HCID仕込み量
反応物4-Fluorobenzoyl chlorideHCID 67879—
反応物[(3SR,4RS)-3-(3,4-Dichloro-phenyl)-4-methylamino-pyrrolidin-1-yl]-[1-(1-methyl-cyclopropanecarbonyl)-piperidin-4-yl]-methanoneHCID 67025815—
生成物N-{(3RS,4SR)-4-(3,4-Dichloro-phenyl)-1-[1-(1-methyl-cyclopropanecarbonyl)-piperidine-4-carbonyl]-pyrrolidin-3-yl}-4-fluoro-N-methyl-benzamideHCID 67025592—

反応手順

In analogy to the procedure described for the synthesis of example 96 (step e), the title compound N-{(3RS,4SR)-4-(3,4-dichloro-phenyl)-1-[1-(1-methyl-cyclopropanecarbonyl)-piperidine-4-carbonyl]-pyrrolidin-3-yl}-4-fluoro-N-methyl-benzamide was prepared from {4-[(3SR,4RS)-3-(3,4-dichloro-phenyl)-4-methylamino-pyrrolidine-1-carbonyl]-piperidin-1-yl}-(1-methyl-cyclopropyl)-methanone using 4-fluorobenzoyl chloride instead of 4-methoxy-3-(trifluoromethyl)benzoyl chloride and was obtained as a light brown foam. MS m/e: 560.1 [M]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08404679B2
出典データセットuspto-grants-2013_03
ORD IDord-87fb259792eb4bbdb04ab80504c74880
出典メモuspto-grants-2013_03