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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 593902생성일: 2026년 10월 24일

Methanol → 6-cyano-3-methyl-1-(1-methylethyl)-1H-indole-4-carboxylic acid

https://huagongshe.com/ko/reaction/593902

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Sodium HydroxideHCID 14798—
반응물methyl 6-cyano-1-isopropyl-3-methyl-1H-indole-4-carboxylateHCID 67467281—
용매TetrahydrofuranHCID 8028—
생성물6-cyano-3-methyl-1-(1-methylethyl)-1H-indole-4-carboxylic acidHCID 6746808964.2%

반응 단계

To a 50 ml round bottom was added methyl 6-cyano-3-methyl-1-(1-methylethyl)-1H-indole-4-carboxylate (230 mg, 0.897 mmol), followed by methanol (1 mL) and THF (1 mL). To the solution was added 3M NaOH (0.449 mL, 2.69 mmol). The reaction stirred at rt for 20 h. The reaction was evaporated and treated with acidic water to pH 5. A brown solid crashed out and was collected by filtration. The solid was an impurity. The pH of the liquid was adjusted to 3 and the liquid was evaporated leaving a residue. Trituration of the residue with water, followed by filtration yielded 6-cyano-3-methyl-1-(1-methylethyl)-1H-indole-4-carboxylic acid (155 mg, 0.576 mmol, 64.2% yield) as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 13.16 (br. s., 1H) 8.33 (s, 1H) 7.78 (s, 1H) 7.66 (s, 1H) 4.81-4.98 (m, 1H) 2.33 (s, 4H) 1.45 (d, J=6.57 Hz, 6H). MS(ES) [M+H]+ 243.3.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09242962B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-f93c731a88cc4e44b9190ace3bfd09f6
출처 메모uspto-grants-2016_01