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HRID 225461作成日:2026年10月25日
4,5-Dichlorophthalic anhydride → 3-(5,6-dichloro-1,3-dioxo-1,3-dihydro-2H-isoindole-2-yl)thiophene-2-carboxamide
https://huagongshe.com/reaction/225461
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4,5-Dichlorophthalic anhydride | HCID 70334 | — |
| 反応物 | 3-Aminothiophene-2-carboxamide | HCID 518993 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | 3-(5,6-dichloro-1,3-dioxo-1,3-dihydro-2H-isoindole-2-yl)thiophene-2-carboxamide | HCID 69074939 | — |
反応手順
3-aminothiophene-2-carboxamide was added to an acetic acid solution of 4,5-dichlorophthalic anhydride and stirred all night heated to reflux to give 3-(5,6-dichloro-1,3-dioxo-1,3-dihydro-2H-isoindole-2-yl)thiophene-2-carboxamide. 1M NaOH aq was added to THF-MeOH solution of the obtained 3-(5,6-dichloro-1,3-dioxo-1,3-dihydro-2H-isoindole-2-yl)thiophene-2-carboxamide and stirred for 2.5 hours at 80° C. to give 4,5-dichloro-2-(4-oxo-3,4-dihydrothieno[3,2-d]pyrimidine-2-yl)benzoic acid. Sulfuric acid was added to a MeOH-1,4-dioxane solution of the obtained 4,5-dichloro-2-(4-oxo-3,4-dihydrothieno[3,2-d]pyrimidine-2-yl)benzoic acid and stirred for three days at 70° C. to give methyl 4,5-dichloro-2-(4-oxo-3,4-dihydrothieno[3,2-d]pyrimidine-2-yl)benzoate.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07557112B2 |
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| 出典データセット | uspto-grants-2009_07 |
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| ORD ID | ord-8036fccdbecc4c7b9099ebc740f635a3 |
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| 出典メモ | uspto-grants-2009_07 |
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