Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 512029생성일: 2026년 10월 27일
Triethylamine → 4-[(5-Chloropyridin-2-yl)methoxy]-2,5-difluoro-N-(methylsulfonyl)benzamide diethylamine salt
https://huagongshe.com/reaction/512029
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Methanesulfonyl chloride | HCID 31297 | — |
| 반응물 | (5-Chloropyridin-2-yl)methanol | HCID 20537893 | — |
| 반응물 | 2,5-difluoro-4-hydroxy-N-(methylsulfonyl)benzamide | HCID 58042416 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-[(5-Chloropyridin-2-yl)methoxy]-2,5-difluoro-N-(methylsulfonyl)benzamide diethylamine salt | HCID 86682567 | — |
반응 단계
To a solution of (5-chloropyridin-2-yl)methanol (15 mg, 0.105 mmol), in dichloromethane (5 mL) and triethylamine (0.02 mL, 0.157 mmol) was added methanesulfonyl chloride (0.01 mL, 0.115 mmol). The reaction was stirred at room temperature for 2 hours. The solvent was removed in vacuo to afford a residue, which was taken up in DMSO (5 mL). Potassium carbonate (43 mg, 0.315 mmol) was added, followed by 2,5-difluoro-4-hydroxy-N-(methylsulfonyl)benzamide (Preparation 110, 29 mg, 0.115 mmol) and the reaction was heated to 50° C. overnight. The reaction mixture was cooled to room temperature, diluted with water (10 mL) and extracted with ethyl acetate (3×10 mL). The combined organic layers were dried over sodium sulphate, filtered and concentrated in vacuo. The resulting residue was purified by preparative HPLC to afford the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09102621B2 |
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| 출처 데이터셋 | uspto-grants-2015_08 |
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| ORD ID | ord-3f891cc096084a35aafa378cfe49e8d8 |
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| 출처 메모 | uspto-grants-2015_08 |
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