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HRID 225271作成日:2026年10月25日

5-Aminoimidazole-4-carboxamide hydrochloride → 4-(m-Methoxyphenyl)imidazo[1,5-a]pyrimidine-8-carboxamide

https://huagongshe.com/reaction/225271

反応式

関与物質

役割名称HCID仕込み量
反応物5-Aminoimidazole-4-carboxamide hydrochlorideHCID 66146—
反応物Sodium AcetateHCID 517045—
反応物3-Dimethylamino-3'-methoxyacrylophenoneHCID 42573796—
溶媒Acetic AcidHCID 176—
生成物4-(m-Methoxyphenyl)imidazo[1,5-a]pyrimidine-8-carboxamideHCID 14677474—

反応手順

A mixture of 1.62 g. of 4-amino-5-imidazolecaboxamide hydrochloride, 3-dimethylamino-3'-methoxyacrylophenone, 0.82 g. of sodium acetate and 25 ml. of glacial acetic acid is refluxed for 10 hours. The mixture is evaporated to dryness and the residue worked up to give 4-(m-methoxyphenyl)imidazo[1,5-a]pyrimidine-8-carboxamide. This compound is treated as for Example 29 with trifluoroacetic anhydride to give the product of the example.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04236005
出典データセットuspto-grants-1980_11
ORD IDord-12c217d117a749b1a77ed7237de14d30
出典メモuspto-grants-1980_11