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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18419생성일: 2026년 10월 25일

Water → N-[5-(3-nitrophenyl)-2,3-dihydro-1H-inden-2-yl]-2-propanesulfonamide

https://huagongshe.com/reaction/18419

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물3-Nitrophenylboronic AcidHCID 1677—
반응물Cesium carbonateHCID 10796—
반응물N-(5-iodo-2,3-dihydro-1H-inden-2-yl)-2-propanesulfonamideHCID 46899809—
촉매TriphenylphosphineHCID 11776—
촉매palladium(II) acetateHCID 167845—
용매1,4-DioxaneHCID 31275—
생성물N-[5-(3-nitrophenyl)-2,3-dihydro-1H-inden-2-yl]-2-propanesulfonamideHCID 46900137109.1%

반응 조건

온도80 °C

반응 단계

A mixture of Intermediate 2 (800 mg, 2.19 mmol) and 3-nitrophenyl boronic acid (366 mg, 2.19 mmol, Sigma Aldrich Company Ltd.) in dioxane (60 ml) was treated with cesium carbonate (1.07 g, 3.29 mmol) and water (20 ml) and degassed with argon for 2 min. Palladium (II) acetate (25 mg, 0.11 mmol) and triphenylphosphine (58 mg, 0.22 mmol) were added and the mixture was stirred at 80° C. under argon for 16 h. The reaction mixture was cooled, then partitioned between ethyl acetate (100 ml) and water (100 ml). The organic layer was separated and dried over Na2SO4 and evaporated in vacuo to give a brown oil (861 mg). This crude oil was purified using flash chromatography to give the title compound as a yellow oil (500 mg, 63%); mass spectrum: (ES−): Found 359 (MH−). C18H20N2O4S requires 360; 1H-NMR (400 MHz, CDCl3) δ 1.38 (6H, m), 2.99 (2H, m), 3.18 (1H, m), 3.38 (2H, m), 4.35 (2H, m), 7.34 (1H, d J=8 Hz), 7.45 (2H, m), 7.60 (1H, m), 7.88 (1H, dd, J=8 Hz and 1 Hz), 8.19 (1H, m), 8.41 (1H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741351B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-1a470015f4bc4716916c32645d9d4aee
출처 메모uspto-grants-2010_06