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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2195741생성일: 2026년 10월 27일

Hydroxylamine → 3-(4-fluoro-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid hydroxyamide

https://huagongshe.com/reaction/2195741

반응식

참여 물질

역할이름HCID투입량
반응물HydroxylamineHCID 787—
반응물Sodium HydroxideHCID 14798—
반응물3-(4-fluoro-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid methyl esterHCID 69449552—
용매WaterHCID 962—
용매MeOH tetrahydrofuranHCID 21899815—
생성물3-(4-fluoro-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid hydroxyamideHCID 2475390250%

반응 단계

To a solution of sodium hydroxide (64 mg, 1.6 mmol) and 50% aqueous hydroxylamine (0.65 mL) was added 3-(4-fluoro-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid methyl ester (58 mg, 0.2 mmol) dissolved in THF/MeOH (1 mL, 1:1). After stirring 4 hr at room temperature, the solution was diluted with water (4 mL) and the volatile solvents were removed in vacuo. The solution was then neutralized to pH=7-8 with 1N HCl and then subjected to HPLC purification to provide 3-(4-fluoro-phenylmethyl)-1-methyl-1H-indole-5-carboxylic acid hydroxyamide (32 mg, 50% yield). 1H NMR (400 MHz, DMSO) δ 11.05 (s, 1H), 8.83 (br s, 1H), 7.97 (s, 1H), 7.57 (dd, 1H, J=1.7, 8.6 Hz), 7.41 (d, 1H, J=8.6 Hz) 7.30 (m, 2H), 7.18 (s, 1H), 7.08 (m, 2H), 4.03 (s, 2H), 3.74 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08338416B2
출처 데이터셋uspto-grants-2012_12
ORD IDord-aafd5d3b5b1b42489b9675d9ba8b09e8
출처 메모uspto-grants-2012_12