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HRID 656425作成日:2026年10月27日

5-tert-butyl-2,3-dihydro-1H-inden-1-amine → N-(5-tert-butyl-2,3-dihydro-1H-inden-1-yl)-N'-5-isoquinolinylurea

https://huagongshe.com/reaction/656425

反応式

関与物質

役割名称HCID仕込み量
反応物5-tert-butyl-2,3-dihydro-1H-inden-1-amineHCID 11506601—
反応物5-IsocyanatoisoquinolineHCID 11586357—
溶媒Diethyl EtherHCID 3283—
生成物N-(5-tert-butyl-2,3-dihydro-1H-inden-1-yl)-N'-5-isoquinolinylureaHCID 11485180—

反応手順

5-tert-Butyl-2,3-dihydro-1H-inden-1-ylamine (150 mg, 1.13 mmol) in diethyl ether (10 mL) was treated with 5-isocyanatoisoquinoline in diethyl ether. The mixture was stirred for 2 hours, filtered, and the filter cake was washed with diethyl ether to provide the title compound. NMR (DMSO-d6) 1.29 (s, 9H), 1.78-1.90 (m, 1H), 2.43-2.54 (m, 1H, buried under DMSO), 2.76-3.05 (m, 2H), 5.19 (m, 1H), 7.27 (m, 2H), 7.31 (m, 1H), 7.43 (d, 1H), 7.89 (t, 1H), 8.05 (d, 1H), 8.63 (d, 1H), 8.69 (d, 1H), 9.33 (s, 1H), 9.73 (s, 1H); MS (ESI+) 360 (M+H)+; Elemental: Calculated for C23H25N3O.HCl.0.5H2O: C, 68.22; H, 6.72; N, 10.38. Found: C, 68.31; H, 6.81; N, 10.16.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08071762B2
出典データセットuspto-grants-2011_12
ORD IDord-7eedeaf1631748a1851cf6fd0532becc
出典メモuspto-grants-2011_12