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HRID 68936作成日:2026年10月25日
2-Amino-4,5,6,7-tetrahydrobenzothiazole → 2-methylsulfanyl-4-oxo-5,6,7,8-tetrahydro-4H-9-thia-1,4a-diaza-fluorene-3-carboxylic acid
https://huagongshe.com/reaction/68936
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Amino-4,5,6,7-tetrahydrobenzothiazole | HCID 18046 | — |
| 反応物 | 5-[Bis(ethylsulfanyl)methylidene]-2,2-dimethyl-1,3-dioxane-4,6-dione | HCID 13679812 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-methylsulfanyl-4-oxo-5,6,7,8-tetrahydro-4H-9-thia-1,4a-diaza-fluorene-3-carboxylic acid | HCID 67117107 | 46.8% |
反応手順
The suspension of 4,5,6,7-tetrahydro-benzothiazol-2-yl-amine (8 gm, 0.0519 mol) and 5-(bis-ethylsulfanyl-methylene)-2,2-dimethyl-[1,3]dioxane-4,6-dione (14.2 gm, 0.0572 mol) in ethanol (60 ml) was heated at 85-90° C. for 10 hours. Reaction mixture was cooled to room temperature and filtered. The solid, thus obtained, was washed with ethanol (20 ml) followed by with diethyl ether (50 ml) and suck dried to give 7.2 gm of title compound as a solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08822484B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-1d8e0f44e55846caa74804a84a556536 |
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| 出典メモ | uspto-grants-2014_09 |
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