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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

反応式

関与物質

役割名称HCID仕込み量
反応物4,5-Dichlorophthalic anhydrideHCID 70334—
反応物3-Aminothiophene-2-carboxamideHCID 518993—
溶媒Acetic AcidHCID 176—
生成物3-(5,6-dichloro-1,3-dioxo-1,3-dihydro-2H-isoindole-2-yl)thiophene-2-carboxamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07557112B2
出典データセットuspto-grants-2009_07
ORD IDord-8036fccdbecc4c7b9099ebc740f635a3
出典メモuspto-grants-2009_07