돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 593523생성일: 2026년 10월 25일

Toluene → 4-(5-Cyano-2-pyridin-3-yl-indole-1-carbonyl)-benzoic acid methyl ester

https://huagongshe.com/reaction/593523

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Methyl 4-(chlorocarbonyl)benzoateHCID 81850—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
반응물2-pyridin-3-yl-1H-indole-5-carbonitrileHCID 44554135—
용매TetrahydrofuranHCID 8028—
생성물4-(5-Cyano-2-pyridin-3-yl-indole-1-carbonyl)-benzoic acid methyl esterHCID 58215547—

반응 단계

To a solution of 2-pyridin-3-yl-1H-indole-5-carbonitrile (Example 8, 240 mg, 1.09 mmol) in THF (10 mL) at room temperature is added 0.5 M KHMDS in toluene (4.0 mL, 2.0 mmol). After 30 min, 4-chlorocarbonyl-benzoic acid methyl ester (400 mg, 2.0 mmol) is added. The mixture is stirred under N2 for 1 h. The reaction is quenched with aqueous sodium bicarbonate and the volatiles are removed in vacuo. Purification by silica gel flash chromatography using a heptane-ethyl acetate gradient affords 4-(5-cyano-2-pyridin-3-yl-indole-1-carbonyl)-benzoic acid methyl ester. 1H NMR (400 MHz, MeOD) δ ppm 3.90 (s, 3H), 7.12 (s, 1H), 7.26 (dd, J=8.0, 4.9 Hz, 1H), 7.63-7.72 (m, 3H), 7.77-7.81 (m, 1H), 7.91-7.96 (m, 3H), 8.17 (d, J=1.5 Hz, 1H), 8.32 (dd, J=4.8, 1.5 Hz, 1H), 8.56 (d, J=2.3 Hz, 1H). HRMS (ESI) m/z 382.1186 [(M+H)+ Calcd for C23H16N3O3: 382.1192].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09242963B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-e58a1b088f1e4327af4b65e806b7e317
출처 메모uspto-grants-2016_01