Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 326712생성일: 2026년 10월 26일
Ethylene Glycol → N-[6-(2-hydroxyethoxy)-5-(o-methoxybenzyl)-4-pyrimidinyl]-p-methoxybenzenesulfonamide
https://huagongshe.com/reaction/326712
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethylene Glycol | HCID 174 | — |
| 반응물 | Sodium Glycolate | HCID 517347 | — |
| 반응물 | Sodium | HCID 5360545 | — |
| 반응물 | HCID 12396954 | HCID 12396954 | — |
| 생성물 | N-[6-(2-hydroxyethoxy)-5-(o-methoxybenzyl)-4-pyrimidinyl]-p-methoxybenzenesulfonamide | HCID 19735392 | — |
반응 단계
300 mg of N-[6-chloro-5-(p-methoxybenzyl)-4-pyrimidinyl]-p-methoxybenzenesulfonamide were added to a sodium glycolate solution from 1 ml of dry ethylene glycol and 46 mg of sodium. The reaction mixture was heated at 125° C. for 4 hours under an argon atmosphere. Thereafter, the ethylene glycol was distilled under reduced pressure. The residue was partitioned between ethyl acetate and 1N hydrochloric acid. The organic phase was washed neutral, dried and evaporated. The residue was chromatographed on silica gel with methylene chloride/ethyl acetate (1:1 v/v). There were obtained 250 mg of N-[6-(2-hydroxyethoxy)-5-(o-methoxybenzyl)-4-pyrimidinyl]-p-methoxybenzenesulfonamide, melting point 161°-162° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05270313 |
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| 출처 데이터셋 | uspto-grants-1993_12 |
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| ORD ID | ord-e0b87538e9714a53aab5aecb6702ad63 |
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| 출처 메모 | uspto-grants-1993_12 |
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