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HRID 1983186作成日:2026年10月26日

5-Methyl-3-phenylisoxazole-4-carboxylic acid → 2-(5-Methyl-3-phenyl-isoxazol-4-yl)-5-thiophen-3-yl-[1,3,4]oxadiazole

https://huagongshe.com/reaction/1983186

反応式

関与物質

役割名称HCID仕込み量
反応物5-Methyl-3-phenylisoxazole-4-carboxylic acidHCID 14343—
反応物Thiophene-3-carbohydrazideHCID 468648—
生成物2-(5-Methyl-3-phenyl-isoxazol-4-yl)-5-thiophen-3-yl-[1,3,4]oxadiazoleHCID 6721576138%

反応手順

As described for example 121, 5-methyl-3-phenylisoxazole-4-carboxylic acid (357 mg, 1.76 mmol) using thiophene-3-carboxylic acid hydrazide instead of thiophene-2-carboxylic acid hydrazide was converted to the title compound (SiO2, heptane:ethyl acetate=90:10 to 60:40, 207 mg, 38%) which was obtained as a yellow semisolid. MS: m/e=310.3 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07541372B2
出典データセットuspto-grants-2009_06
ORD IDord-68f5e694037b4fa8a3197d93ec079673
出典メモuspto-grants-2009_06