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HRID 1873735作成日:2026年10月27日

Bromobenzene → N-(5-ethyl-1,3,4-thiadiazol-2-yl)-1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxamide

https://huagongshe.com/reaction/1873735

反応式

関与物質

役割名称HCID仕込み量
反応物BromobenzeneHCID 7961—
反応物2-Amino-5-ethyl-1,3,4-thiadiazoleHCID 26444—
反応物Ethyl 1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxylateHCID 57619607—
生成物N-(5-ethyl-1,3,4-thiadiazol-2-yl)-1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxamideHCID 6720180375%

反応手順

212 mg of ethyl 1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxylate and 117 mg of 2-amino-5-ethyl-1,3,4-thiadiazole were added to 2.5 ml of bromobenzene, then, the mixture was stirred for 5 hours under heat refluxing condition. The reaction mixture was cooled to room temperature. The resulting solid was collected by filtration, and washed with a mixed solvent of t-butyl methyl ether and hexane and dried to obtain 200 mg of N-(5-ethyl-1,3,4-thiadiazol-2-yl)-1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxamide (hereinafter, referred to as present compound 17) represented by the formula:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08304437B2
出典データセットuspto-grants-2012_11
ORD IDord-97b32844e5c344818b7587a9318f9623
出典メモuspto-grants-2012_11