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HRID 326712作成日:2026年10月26日
Ethylene Glycol → N-[6-(2-hydroxyethoxy)-5-(o-methoxybenzyl)-4-pyrimidinyl]-p-methoxybenzenesulfonamide
https://huagongshe.com/reaction/326712
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Ethylene Glycol | HCID 174 | — |
| 反応物 | Sodium Glycolate | HCID 517347 | — |
| 反応物 | Sodium | HCID 5360545 | — |
| 反応物 | HCID 12396954 | HCID 12396954 | — |
| 生成物 | N-[6-(2-hydroxyethoxy)-5-(o-methoxybenzyl)-4-pyrimidinyl]-p-methoxybenzenesulfonamide | HCID 19735392 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05270313 |
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| 出典データセット | uspto-grants-1993_12 |
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| ORD ID | ord-e0b87538e9714a53aab5aecb6702ad63 |
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| 出典メモ | uspto-grants-1993_12 |
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