Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 248023생성일: 2026년 10월 26일
Sodium Chloride → N-(2-Pyridinylmethyl)-N-[[4-(tetradecyloxy)phenyl]methyl]methanesulfonamide
https://huagongshe.com/reaction/248023
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Chloride | HCID 5234 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | N-(pyridin-2-ylmethyl)methanesulfonamide | HCID 4657001 | — |
| 반응물 | 1-(Bromomethyl)-4-(tetradecyloxy)benzene | HCID 10022840 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-(2-Pyridinylmethyl)-N-[[4-(tetradecyloxy)phenyl]methyl]methanesulfonamide | HCID 19014986 | 38.3% |
반응 단계
To a room temperature slurry of 0.391 g of 50% sodium hydride in 20 ml of dry tetrahydrofuran is added, via cannula, 1.27 g of product from Example 121 in 30 ml of dry tetrahydrofuran. The reaction is stirred at room temperature for 1.5 hours. Two and one half grams of product from Example 20 in 30 ml of dry tetrahydrofuran is added via cannula. The reaction is stirred at room temperature for 20 hours followed by heating at reflux temperature for 2 hours. The cooled reaction is poured into half saturated sodium chloride and extracted with methylene chloride. The combined organic layers are washed with saturated sodium chloride, dried and concentrated in vacuo. The residue is purified by chromatography (silica gel: 40% ethyl acetate/hexane) to give 1.22 g of the desired product as colorless crystals.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05208247 |
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| 출처 데이터셋 | uspto-grants-1993_05 |
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| ORD ID | ord-81fb874163f54816a4261f6a54b2ed94 |
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| 출처 메모 | uspto-grants-1993_05 |
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