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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133597생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/133597

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylcarbodiimideHCID 12734—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물3-Bromo-4-methylbenzoic acidHCID 82130—
반응물1-(4-Chlorobenzyl)-4-((glycylamino)methyl}piperidineHCID 18426155—
용매ChloroformHCID 6212—
용매tert-ButanolHCID 6386—
생성물4-[[N-(3-bromo-4-methylbenzoyl)glycyl]aminomethyl]-1-(4-chlorobenzyl)piperidineHCID 18426237—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390830B1
출처 데이터셋uspto-grants-2008_06
ORD IDord-fac85c040d5049d0afcd61252ffa636f
출처 메모uspto-grants-2008_06