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HRID 24695作成日:2026年10月27日

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

https://huagongshe.com/reaction/24695

反応式

関与物質

役割名称HCID仕込み量
反応物SuccinimideHCID 11439—
反応物TriphenylphosphineHCID 11776—
反応物Diethyl azodicarboxylateHCID 5462977—
反応物N-(2,6-dichlorobenzoyl)-4-[2,6-dimethoxy-4-(hydroxymethyl)phenyl]-L-phenylalanine tert-butyl esterHCID 54401991—
溶媒TetrahydrofuranHCID 8028—
生成物N-(2,6-dichlorobenzoyl)-4-[2,6-dimethoxy-4-(succinimidomethyl)phenyl]-L-phenylalanine tert-butyl esterHCID 2297062548.2%

反応条件

温度0 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06855843B2
出典データセットuspto-grants-2005_02
ORD IDord-56c872874e3840c7b4386e443eca2318
出典メモuspto-grants-2005_02