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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 500669생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/500669

반응식

참여 물질

역할이름HCID투입량
반응물(Methoxycarbonylsulfamoyl)triethylammonium hydroxideHCID 11032497—
반응물Ethyl 6-{2-[2-(4-methoxybenzoyl)hydrazino]-2-oxoethyl}-1-benzothiophene-2-carboxylateHCID 59424237—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 6-{[5-(4-methoxyphenyl)-1,3,4-oxadiazol-2-yl]methyl}-benzothiophene-2-carboxylateHCID 5942423494%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772238B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-251e4cdac0f443e7ac30a0e81931bdf7
출처 메모uspto-grants-2010_08