Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 605213생성일: 2026년 10월 25일
Potassium Carbonate → {4-[4-(5-Chloro-pyridin-2-ylcarbamoyl)-2-nitro-phenoxy]-phenyl}-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/605213
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 4-chloro-N-(5-chloropyridin-2-yl)-3-nitrobenzamide | HCID 693095 | — |
| 반응물 | N-Boc-4-hydroxyaniline | HCID 2756771 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | {4-[4-(5-Chloro-pyridin-2-ylcarbamoyl)-2-nitro-phenoxy]-phenyl}-carbamic acid tert-butyl ester | HCID 67040773 | 61% |
반응 단계
A solution of the product of Example 199A (300 mg, 0.9612 mmol) in anhydrous N,N-dimethylformamide (5 mL) was treated with N-Boc-4-hydroxyaniline (201 mg, 0.9612 mmol) and potassium carbonate (266 mg, 1.922 mmol) at room temperature, then heated at 80° C. under a nitrogen atmosphere for 5 hours. The reaction was cooled to room temperature and the solvent removed by rotary evaporation in vacuo. The residue was taken up in ethyl acetate (100 mL) and washed with water (4×50 mL) and brine (50 mL). The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated by rotary evaporation in vacuo. Trituration with 5% ethyl acetate gave the title compound (284 mg, 61%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07910595B2 |
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| 출처 데이터셋 | uspto-grants-2011_03 |
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| ORD ID | ord-c8749a8574984cab809137d791ee5269 |
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| 출처 메모 | uspto-grants-2011_03 |
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