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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 24695생성일: 2026년 10월 25일

Succinimide → N-(2,6-dichlorobenzoyl)-4-[2,6-dimethoxy-4-(succinimidomethyl)phenyl]-L-phenylalanine tert-butyl ester

https://huagongshe.com/reaction/24695

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참여 물질

역할이름HCID투입량
반응물SuccinimideHCID 11439—
반응물TriphenylphosphineHCID 11776—
반응물Diethyl azodicarboxylateHCID 5462977—
반응물N-(2,6-dichlorobenzoyl)-4-[2,6-dimethoxy-4-(hydroxymethyl)phenyl]-L-phenylalanine tert-butyl esterHCID 54401991—
용매TetrahydrofuranHCID 8028—
생성물N-(2,6-dichlorobenzoyl)-4-[2,6-dimethoxy-4-(succinimidomethyl)phenyl]-L-phenylalanine tert-butyl esterHCID 2297062548.2%

반응 조건

온도0 °C

반응 단계

DEAD (0.13 mL) was added to an ice-cooled solution of N-(2,6-dichlorobenzoyl)-4-[2,6-dimethoxy-4-(hydroxymethyl)phenyl]-L-phenylalanine tert-butyl ester (250 mg), triphenylphosphine (175 mg) and succinimide (90 mg) in THF (3 mL) under N. The mixture was stirred at 0° C. for 30 min, and warmed to room temperature and stirred for 2 h. The mixture was partitioned between H2O and EtOAc, and the aqueous layer was extracted with EtOAC. The combined organic layer was dried (MgSO4), and concentrated in vacuo. The residue was purified by preparative TLC (silica gel; eluent: EtOAc/hexane 1:1) to give N-(2,6-dichlorobenzoyl)-4-[2,6-dimethoxy-4-(succinimidomethyl)phenyl]-L-phenylalanine tert-butyl ester (138 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855843B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-56c872874e3840c7b4386e443eca2318
출처 메모uspto-grants-2005_02