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HRID 1760292作成日:2026年10月26日

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

https://huagongshe.com/reaction/1760292

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Lawesson's reagentHCID 87949—
反応物5-(2'-oxospiro[cyclohexane-1,3'-[3H]indol]-5'-yl)-1-methyl-pyrrole-2-carbonitrileHCID 21986251—
溶媒TolueneHCID 1140—
生成物5-(2'-Thioxospiro[cyclohexane-1,3'-[3H]indol]-5'-YL)-1-methyl-pyrrole-2-carbonitrileHCID 992713090.5%

反応条件

温度80 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06841568B2
出典データセットuspto-grants-2005_01
ORD IDord-d24817a98d454f0d8242626b1986ba07
出典メモuspto-grants-2005_01