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HRID 1041888作成日:2026年10月26日

4-(Bromomethyl)benzoic acid → 4-((1-Methylspiro[indolin-3,4'-piperidin]-1'-yl)methyl)benzoic acid

https://huagongshe.com/reaction/1041888

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Bromomethyl)benzoic acidHCID 22599—
反応物DiisopropylethylamineHCID 81531—
反応物1-Methyl-1,2-dihydrospiro[indole-3,4'-piperidine]HCID 10655739—
溶媒EthanolHCID 702—
生成物4-((1-Methylspiro[indolin-3,4'-piperidin]-1'-yl)methyl)benzoic acidHCID 70926855142.5%

反応手順

A mixed solution of 1-methylspiro[indolin-3,4′-piperidine] (1.0 g) synthesized according to a method described in [WO 2011/046851 pamphlet, (preparation 15)], 4-(bromomethyl)benzoic acid (1.08 g), and N,N-diisopropylethylamine (2.61 mL) in ethanol (20 mL) was heated and refluxed for 2 hours. To the resultant reaction mixture, N,N-diisopropylethylamine (1.04 mL) was further added, and the resultant reaction mixture was heated and refluxed for 2 hours. The reaction solution was left to reach room temperature, and from the reaction solution, the solvent was distilled off under reduced pressure to obtain a mixture (2.37 g) containing the subject compound. The resultant mixture was used in the next reaction without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08557766B2
出典データセットuspto-grants-2013_10
ORD IDord-461db4dc48d640459cb2cd64094927f0
出典メモuspto-grants-2013_10