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HRID 351849作成日:2026年10月24日
Dimethyl-p-toluidine → 2-Chloro-4-(2,4-dimethoxy-benzyl)-7-methylsulfanyl-3,4-dihydro-benzo[e][1,4]diazepin-5-one
https://huagongshe.com/ja/reaction/351849
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethyl-p-toluidine | HCID 7471 | — |
| 反応物 | Phosphorus oxychloride | HCID 24813 | — |
| 反応物 | 4-(2,4-Dimethoxy-benzyl)-7-methylsulfanyl-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione | HCID 22713482 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 2-Chloro-4-(2,4-dimethoxy-benzyl)-7-methylsulfanyl-3,4-dihydro-benzo[e][1,4]diazepin-5-one | HCID 22713484 | — |
反応手順
4-(2,4-Dimethoxy-benzyl)-7-methylsulfanyl-3,4-dihydro-1H-benzo[e][1,4]diazepine-2,5-dione (630 mg, 1.7 mmol) and N,N-dimethyl-p-toluidine (489 μL, 3.4 mmol) were mixed in toluene (5 mL) and heated to 100° C. Then phosphorus oxychloride (170 μL, 1.9 mmol) was added dropwise and heating at 100° C. was continued for 1 h. The resulting dark red solution was used directly in the subsequent step.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06743789B2 |
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| 出典データセット | uspto-grants-2004_06 |
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| ORD ID | ord-be20683897304400a6363b07e996b88e |
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| 出典メモ | uspto-grants-2004_06 |
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