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HRID 600441作成日:2026年10月24日

alpha-Methyl-3-pyridinemethanol → 3-(6-chloro-8-oxo-9-(1-(pyridin-3-yl)ethyl)-8,9-dihydro-7H-purin-2-yl)-3H-benzo[d]imidazole-5-carbonitrile

https://huagongshe.com/ja/reaction/600441

反応式

関与物質

役割名称HCID仕込み量
反応物alpha-Methyl-3-pyridinemethanolHCID 101192—
反応物3-(6-chloro-8-oxo-8,9-dihydro-7H-purin-2-yl)-3H-benzo[d]imidazole-5-carbonitrileHCID 57612742—
生成物3-(6-chloro-8-oxo-9-(1-(pyridin-3-yl)ethyl)-8,9-dihydro-7H-purin-2-yl)-3H-benzo[d]imidazole-5-carbonitrileHCID 5761274026%

反応手順

Yellow oil (26% yield based on 73% conversion). Synthesized using 1-pyridin-3-yl-ethanol and 3-(6-chloro-8-oxo-8,9-dihydro-7H-purin-2-yl)-3H-benzo[d]imidazole-5-carbonitrile. 1H NMR (300 MHz, CD3OD) δ, ppm: 9.27 (s, 1H), 9.20-9.00 (br m, 1H), 8.86 (d, 1H), 8.88-8.77 (m, 1H, overlapping with 8.86 ppm), 8.68 (s, 1H), 8.13 (br s, 1H), 7.87 (d, 1H), 7.68 (d, 1H), 6.17 (q, J=7.1 Hz, 1H), 2.19 (d, J=7.3 Hz, 3H); MS (EI) m/z 417.1 (MH)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07902187B2
出典データセットuspto-grants-2011_03
ORD IDord-7cba0372b52e4a33b872b18f7ed08ea6
出典メモuspto-grants-2011_03