戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 500669作成日:2026年10月26日

(Methoxycarbonylsulfamoyl)triethylammonium hydroxide → Ethyl 6-{[5-(4-methoxyphenyl)-1,3,4-oxadiazol-2-yl]methyl}-benzothiophene-2-carboxylate

https://huagongshe.com/reaction/500669

反応式

関与物質

役割名称HCID仕込み量
反応物(Methoxycarbonylsulfamoyl)triethylammonium hydroxideHCID 11032497—
反応物Ethyl 6-{2-[2-(4-methoxybenzoyl)hydrazino]-2-oxoethyl}-1-benzothiophene-2-carboxylateHCID 59424237—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 6-{[5-(4-methoxyphenyl)-1,3,4-oxadiazol-2-yl]methyl}-benzothiophene-2-carboxylateHCID 5942423494%

反応手順

A solution of ethyl 6-{2-[2-(4-methoxybenzoyl)hydrazino]-2-oxoethyl}-1-benzothiophene-2-carboxylate (78 mg, 0.19 mmol) and (methoxycarbonylsulfamoyl)-triethylammonium hydroxide, inner salt (113 mg, 0.47 mmol) in THF was heated to 100° C. in the microwave for 10 minutes. The reaction was filtered through a pad of silica and washed with ethyl acetate. The organics were evaporated to dryness to give 70 mg (94%) of the title compound as a clear oil. LC/MS (EI): cal'd 395.1 (MW), exp 395.1 (MW).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07772238B2
出典データセットuspto-grants-2010_08
ORD IDord-251e4cdac0f443e7ac30a0e81931bdf7
出典メモuspto-grants-2010_08