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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53563생성일: 2026년 10월 23일

Indole-3-Butyric Acid → N-Methyl-N-Methoxy-4-(3-indolyl)butyramide

https://huagongshe.com/ko/reaction/53563

반응식

참여 물질

역할이름HCID투입량
반응물Indole-3-Butyric AcidHCID 8617—
반응물N,N-dimethylhydroxylamine hydrochlorideHCID 27969—
반응물DiisopropylethylamineHCID 81531—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
용매AcetonitrileHCID 6342—
생성물N-Methyl-N-Methoxy-4-(3-indolyl)butyramideHCID 1110763194.3%

반응 단계

To a slurry of 1.75 g (8.61 mmol) of 3-indolebutyric acid (Aldrich Chemical Co.) in acetonitrile at room temperature was added 7.0 mL (40.2 mmol) of N,N-diisopropylethylamine, 1.0 g (10.3 mmol) of N,N-dimethylhydroxylamine hydrochloride and 4.19 g (9.5 mmol) of benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (BOP reagent) and the resulting mixture was allowed to stir at room temperature overnight and was then concentrated to dryness. The residue was dissolved into ethyl acetate and washed with water, 0.5N HCl, saturated NaHCO3 and brine and then dried over MgSO4 and concentrated. Flash chromatography (elution with a gradient of 2-10% ether in methylene chloride) provided 2.0 g of the amide 139. 1H NMR consistent with structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05620971
출처 데이터셋uspto-grants-1997_04
ORD IDord-335b9dd89de54030898409aded9b82d1
출처 메모uspto-grants-1997_04