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HRID 133597作成日:2026年10月26日

Diisopropylcarbodiimide → 4-[[N-(3-bromo-4-methylbenzoyl)glycyl]aminomethyl]-1-(4-chlorobenzyl)piperidine

https://huagongshe.com/reaction/133597

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylcarbodiimideHCID 12734—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物3-Bromo-4-methylbenzoic acidHCID 82130—
反応物1-(4-Chlorobenzyl)-4-((glycylamino)methyl}piperidineHCID 18426155—
溶媒ChloroformHCID 6212—
溶媒tert-ButanolHCID 6386—
生成物4-[[N-(3-bromo-4-methylbenzoyl)glycyl]aminomethyl]-1-(4-chlorobenzyl)piperidineHCID 18426237—

反応手順

3-Bromo-4-methylbenzoic acid (0.060 mmol), diisopropylcarbodiimide (0.060 mmol) and HOBt (0.060 mmol) were added to a solution of 1-(4-chlorobenzyl)-4-[(glycylamino)methyl]piperidine (0.050 mmol) in chloroform (1.35 mL) and tert-butanol (0.15 mL). The resulting reaction mixture was stirred at room temperature for 15 hours. The mixture was then loaded onto a Varian™ SCX column and washed with methanol/chloroform=1:1 (12 mL) and methanol (12 mL). The obtained crude product was eluted with a 2 M methanol solution of NH3 (5 mL) and concentrated to thereby afford 4-[[N-(3-bromo-4-methylbenzoyl)glycyl]aminomethyl]-1-(4-chlorobenzyl)piperidine (Compd. No. 1113) (16.1 mg, 65%). The purity was determined by RPLC/MS (95%). ESI/MS m/e 494.0 (C23H27BrClN3O2).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07390830B1
出典データセットuspto-grants-2008_06
ORD IDord-fac85c040d5049d0afcd61252ffa636f
出典メモuspto-grants-2008_06