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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1519941생성일: 2026년 10월 27일

Dichloromethane → N-(3-(N-hydroxycarbamimidoyl)thiophen-2-yl)-2-(4-methoxyphenyl)acetamide

https://huagongshe.com/reaction/1519941

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물TriethylamineHCID 8471—
반응물Hydroxyamine hydrochlorideHCID 443297—
반응물N-(3-cyanothiophen-2-yl)-2-(4-methoxyphenyl)acetamideHCID 2404093—
용매EthanolHCID 702—
용매Sodium BicarbonateHCID 516892—
생성물N-(3-(N-hydroxycarbamimidoyl)thiophen-2-yl)-2-(4-methoxyphenyl)acetamideHCID 136414311—

반응 단계

To a solution of N-(3-cyanothiophen-2-yl)-2-(4-methoxyphenyl)acetamide (234 mg, 0.859 mmol) in a mixture of ethanol (5 mL), methylene chloride (0.5 mL) and triethylamine (202 μL, 1.46 mmol) was added hydroxylamine hydrochloride (90 mg, 1.29 mmol). The resulting solution was stirred at room temperature for 18 h and was subsequently diluted with saturated aqueous sodium bicarbonate and extracted with ethyl acetate. The organic phases were combined, dried (Na2SO4), filtered, concentrated under vacuum and purified on a silica gel column (eluant hexane/ethyl acetate, 7/3 to 2/8) to give N-(3-(N′-hydroxycarbamimidoyl)thiophen-2-yl)-2-(4-methoxyphenyl)acetamide. Retention time (min)=1.161, method [1], MS(ESI) 306.1 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09073891B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-9a58c8edd7d643c793c36081ad1373fd
출처 메모uspto-grants-2015_07