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HRID 601307作成日:2026年10月25日
1-amino-3-[7-(benzyloxy)-1,1-dioxido-4H-1,2,4-benzothiadiazin-3-yl]-4-hydroxyquinolin-2(1H)-one → 3-[7-(benzyloxy)-1,1-dioxido-4H-1,2,4-benzothiadiazin-3-yl]-4-hydroxy-1-{[2-methylpropylidene]amino}quinolin-2(1H)-one
https://huagongshe.com/reaction/601307
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1-amino-3-[7-(benzyloxy)-1,1-dioxido-4H-1,2,4-benzothiadiazin-3-yl]-4-hydroxyquinolin-2(1H)-one | HCID 136358484 | — |
| 溶媒 | Dimethylacetamide | HCID 31374 | — |
| 生成物 | 3-[7-(benzyloxy)-1,1-dioxido-4H-1,2,4-benzothiadiazin-3-yl]-4-hydroxy-1-{[2-methylpropylidene]amino}quinolin-2(1H)-one | HCID 136358487 | 169.4% |
反応手順
The product of Example 304F (0.150 g, 0.32 mmol) and isobutyrlaldehyde (0.44 mL, 4.84 mmol) in N,N-dimethylacetamide (1.5 mL) were reacted at 125° C. for 40 minutes in a microwave reactor in a sealed tube. The reaction was concentrated under a stream of nitrogen warmed through a manifold heated to 165° C. The resulting residue was triturated with diethyl ether and filtered to give the title compound (0.140 g, 84%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07902203B2 |
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| 出典データセット | uspto-grants-2011_03 |
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| ORD ID | ord-48361b71a4bb4ea29a612de9662818b7 |
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| 出典メモ | uspto-grants-2011_03 |
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