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HRID 1391294作成日:2026年10月26日

Pyruvic Acid → 2',5-dichloro-3-(3-pyruvamidomethyl-5-methyl-4H-1,2,4-triazol-4-yl)-benzophenone

https://huagongshe.com/reaction/1391294

反応式

関与物質

役割名称HCID仕込み量
反応物Pyruvic AcidHCID 1060—
反応物Thionyl ChlorideHCID 24386—
反応物Sodium BicarbonateHCID 516892—
反応物2',5-dichloro-3-(3-aminomethyl-5-methyl-4H-1,2,4-triazol-4-yl)-benzophenone dihydrobromideHCID 21325684—
溶媒BenzeneHCID 241—
溶媒ChloroformHCID 6212—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物2',5-dichloro-3-(3-pyruvamidomethyl-5-methyl-4H-1,2,4-triazol-4-yl)-benzophenoneHCID 2132574464.8%

反応手順

A solution of pyruvic acid (0.33 g) and thionyl chloride (0.27 g) in chloroform (2 ml) is refluxed for 1 hour. After cooling, the solution is mixed with 2',5-dichloro-3-(3-aminomethyl-5-methyl-4H-1,2,4-triazol-4-yl)-benzophenone dihydrobromide (1.31 g), benzene (6 ml) and dimethylformamide (11 ml) at 0° C. The resultant mixture is stirred at room temperature for 3 hours and allowed to stand overnight. The reaction mixture is neutralized with aqueous sodium bicarbonate and shaken with ethyl acetate. The organic layer is washed with water, dried and evaporated to remove the solvent. The residue is recrystallized from ethyl acetate to give 2',5-dichloro-3-(3-pyruvamidomethyl-5-methyl-4H-1,2,4-triazol-4-yl)-benzophenone (0.7 g) as crystals melting at 178° to 180° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04141901
出典データセットuspto-grants-1979_02
ORD IDord-1e57b65681de4c05acbdc36eeb8a3a61
出典メモuspto-grants-1979_02