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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Diisopropylcarbodiimide | HCID 12734 | — |
| 반응물 | 1-(4-hydroxyphenyl)-1H-pyrrole-2,5-dione | HCID 81734 | — |
| 반응물 | 3-(4,5-Dimethoxy-2-nitro-benzyloxycarbonylamino)-butyric acid | HCID 59336635 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-(4,5-Dimethoxy-2-nitro benzyloxycarbonyl-amino)-butyric acid 4-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-phenyl ester | HCID 59336582 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07727713B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-ef4d96badb8b48f0bcb90ff68efff15e |
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| 출처 메모 | uspto-grants-2010_06 |
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