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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9317생성일: 2026년 10월 24일

Water → 5-(2'-Thioxospiro[cyclohexane-1,3'-[3H]indol]-5'-YL)-1-methyl-pyrrole-2-carbonitrile

https://huagongshe.com/ko/reaction/9317

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Lawesson's reagentHCID 87949—
반응물5-(2'-oxospiro[cyclohexane-1,3'-[3H]indol]-5'-yl)-1-methyl-pyrrole-2-carbonitrileHCID 21986251—
용매TolueneHCID 1140—
생성물5-(2'-Thioxospiro[cyclohexane-1,3'-[3H]indol]-5'-YL)-1-methyl-pyrrole-2-carbonitrileHCID 992713090.5%

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온도80 °C

반응 단계

To a solution of 5-(2′-oxospiro[cyclohexane-1,3′-[3H]indol]-5′-yl)-1-methyl-pyrrole-2-carbonitrile (0.55 g, 1.8 mmol, 1 eq) in toluene (50 mL) was added Lawesson's reagent (0.47 g, 1.1 mmol, 0.65 eq) and the reaction was heated to 80° C. for 1 hour. The reaction was cooled to room temperature, poured into water (100 mL) and extracted with ethyl acetate (2×100 mL). The organic layers were combined, washed with brine (50 mL), dried over magnesium sulfate, filtered and concentrated in vacuo. Purification by flash column chromatography on silica gel gave the product as a white solid (0.32 g, 55%). 1H NMR (d6-DMSO, 500 MHz) δ 1.36–1.99 (m, 10 H), 3.7 (s, 3 H), 6.35 (d, 1 H, J=4.2 Hz), 7.05 (d, 1 H, J=4.2 Hz), 7.16 (d, 1 H, J=7.9 Hz), 7.44 (dd, 1 H, J=1.6, 8.1 Hz), 7.83 (d, 1 H, J=1.6 Hz), 12.75 (s, 1 H). MS (ESI) [M−H]−=320. Anal. calcd. for C19H19N3S: C, 70.99; H, 5.96; N, 13.07. Found: C, 68.69; H, 5.36; N, 12.27.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091234B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-70f66bc6736f4a80ac413ff2db27ac21
출처 메모uspto-grants-2006_08