Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37096생성일: 2026년 10월 24일
Sodium Glycolate → 4-tert-butyl-N-[5-(2-chloro-5methoxy-phenoxy)-6-(2-hydroxy-ethoxymethyl)-2-(morpholin-4-yl)-pyrimidin-4-yl]-benzenesulphonamide
https://huagongshe.com/ko/reaction/37096
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Sodium Glycolate | HCID 517347 | — |
| 반응물 | Sodium | HCID 5360545 | — |
| 반응물 | 4-tert-butyl-N-[5-(2-chloro-5-methoxy-phenoxy)-6-chloromethyl-2-(morpholin-4-yl)-pyrimidin-4-yl]-benzenesulphonamide | HCID 19934755 | — |
| 용매 | Ethylene Glycol | HCID 174 | — |
| 생성물 | 4-tert-butyl-N-[5-(2-chloro-5methoxy-phenoxy)-6-(2-hydroxy-ethoxymethyl)-2-(morpholin-4-yl)-pyrimidin-4-yl]-benzenesulphonamide | HCID 9830283 | — |
반응 단계
1 g of 4-tert-butyl-N-[5-(2-chloro-5-methoxy-phenoxy)-6-chloromethyl-2-(morpholin-4-yl)-pyrimidin-4-yl]-benzenesulphonamide was added to a sodium glycolate solution from 2.5 g of ethylene glycol and 0.12 g of sodium. The reaction mixture was stirred at 80° C. under argon for 72 hours. Thereafter, the ethylene glycol was distilled off and the residue was partitioned between ethyl acetate and 1 N hydrochloric acid. The organic phase was washed with water, dried over sodium sulphate and the solvent was distilled off. The residue was chromatographed over silica gel with ether. There was obtained 0.85g of 4-tert-butyl-N-[5-(2-chloro-5methoxy-phenoxy)-6-(2-hydroxy-ethoxymethyl)-2-(morpholin-4-yl)-pyrimidin-4-yl]-benzenesulphonamide. m.p 162°-164° C., MS: M=606.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05420129 |
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| 출처 데이터셋 | uspto-grants-1995_05 |
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| ORD ID | ord-8af9041743f64ffb915679f0890fb30c |
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| 출처 메모 | uspto-grants-1995_05 |
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