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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 913185생성일: 2026년 10월 26일

Sodium Hydroxide → N-(3-methylisothiazol-5-yl)-2-[1-(3-methylisoxazol-5-ylmethyl)-1H-indol-3-yl]-2-oxoacetamide

https://huagongshe.com/reaction/913185

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물3-Methylisothiazol-5-amineHCID 32307—
반응물Oxalyl chlorideHCID 65578—
반응물5-[(1-Indolyl)methyl]-3-methylisoxazoleHCID 11275877—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
용매TriethylamineHCID 8471—
생성물N-(3-methylisothiazol-5-yl)-2-[1-(3-methylisoxazol-5-ylmethyl)-1H-indol-3-yl]-2-oxoacetamideHCID 10293154—

반응 조건

온도0 °C

반응 단계

A solution of 5-(1H-1-indolylmethyl)-3-methylisoxazole (212 mg, 1.0 mmol) in 10 mL diethyl ether was added to oxalyl chloride (254 mg, 2.0 mmol) dropwise at 0° C. The reaction mixture was stirred at 0° C. for 3 hours and then the reaction solvent was evaporated. The residue was dissolved in 5 mL tetrahydrofuran and then the 3-methyl-5-isothiazolamine (114 mg, 1.0 mmol) and triethylamine (1 mL) in 10 mL tetrahydrofuran was added dropwise. The mixture was stirred for 10 hours and then 1 N NaOH (4 mL) was added to the reaction flask dropwise. The mixture was extracted three times with a total of 60 mL of tetrahydrofuran, the organic phase was dried using anhydrous magnesium sulfate and filtered, and the filtrate was concentrated in vacuum. The residue was crystallized from methanol. Yield: 0.27 g, 71%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08026271B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-90f023475c684d8ba878bdf3b848dffe
출처 메모uspto-grants-2011_09