化工社化工社 化学情報印刷レポート · 研究参考用
HRID 607400作成日:2026年10月25日
N,N-Diethylethylenediamine → (S)-N-[(2-{[2-(diethylamino)ethyl]amino}-2-oxoethyl)(oxo)phenyl-lambda6-sulfanylidene]-5-[(3-hydroxyphenyl)ethynyl]nicotinamide
https://huagongshe.com/reaction/607400
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | N,N-Diethylethylenediamine | HCID 60993 | — |
| 反応物 | (S)-Ethyl[N-({5-[(3-hydroxyphenyl)ethynyl]pyridin-3-yl}carbonyl)-S-phenylsulfonimidoyl]acetate | HCID 86629474 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | (S)-N-[(2-{[2-(diethylamino)ethyl]amino}-2-oxoethyl)(oxo)phenyl-lambda6-sulfanylidene]-5-[(3-hydroxyphenyl)ethynyl]nicotinamide | HCID 24954918 | 60.3% |
反応手順
(S)-Ethyl[N-({5-[(3-hydroxyphenyl)ethynyl]pyridin-3-yl}carbonyl)-S-phenylsulfonimidoyl]acetate (73 mg, 0.16 mmol) in anhydrous MeOH (1.5 mL) was added N,N-diethylethylenediamine (0.12 mL, 0.84 mmol) dropwise. The reaction mixture was heated at 30° C. for 4 hours. The reaction mixture was evaporated and the residue was partitioned between EtOAc and saturated aqueous NaHCO3. The organic layer was washed once with brine, dried (anhydrous Na2SO4), concentrated. The residue was purified by chromatography (silica gel, 50:1 CHCl3:MeOH to 10:1 CHCl3:MeOH). The product containing fractions were concentrated to give the title compound as a foamy solid (50 mg, 59%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07915443B2 |
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| 出典データセット | uspto-grants-2011_03 |
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| ORD ID | ord-58740cf5ba7344e0b3dc77ceec184c34 |
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| 出典メモ | uspto-grants-2011_03 |
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