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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12013생성일: 2026년 10월 24일

Diisopropylcarbodiimide → 3-(4,5-Dimethoxy-2-nitro benzyloxycarbonyl-amino)-butyric acid 4-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-phenyl ester

https://huagongshe.com/ko/reaction/12013

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylcarbodiimideHCID 12734—
반응물1-(4-hydroxyphenyl)-1H-pyrrole-2,5-dioneHCID 81734—
반응물3-(4,5-Dimethoxy-2-nitro-benzyloxycarbonylamino)-butyric acidHCID 59336635—
용매TetrahydrofuranHCID 8028—
생성물3-(4,5-Dimethoxy-2-nitro benzyloxycarbonyl-amino)-butyric acid 4-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-phenyl esterHCID 59336582—

반응 조건

온도0 °C

반응 단계

1-(4-Hydroxy-phenyl)-pyrrole-2,5-dione (1 mmol), NHS (1.0 mmol) and 3-(4,5-dimethoxy-2-nitro-benzyloxycarbonylamino)-butyric acid (1 mmol) is dissolved in THF (3 mL). The solution is cooled to 0° C. and treated dropwise with DIC (1.2 mmol). The cooling bath is removed after 1 hour and the reaction mixture is left at room temperature o/n. The solvent is evaporated in vacuo and the pure product (3-(4,5-dimethoxy-2-nitro benzyloxycarbonyl-amino)-butyric acid 4-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-phenyl ester) is isolated by silica column purification using EtOAc-heptane (1:4 then 1:2 then 1:1) as eluent.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727713B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-ef4d96badb8b48f0bcb90ff68efff15e
출처 메모uspto-grants-2010_06