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HRID 17205作成日:2026年10月25日

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-YL)thiophene-2-carbaldehyde → N-{4-[4-amino-7-(2-formylthien-3-yl)thieno[3,2-c]pyridin-3-yl]-2-methoxyphenyl}-1-methyl-1H-indole-2-carboxamide

https://huagongshe.com/reaction/17205

反応式

関与物質

役割名称HCID仕込み量
反応物3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-YL)thiophene-2-carbaldehydeHCID 18450673—
反応物N-[4-(4-amino-7-iodothieno[3,2-c]pyridin-3-yl)-2-methoxyphenyl]-1-methyl-1H-indole-2-carboxamideHCID 18451298—
生成物N-{4-[4-amino-7-(2-formylthien-3-yl)thieno[3,2-c]pyridin-3-yl]-2-methoxyphenyl}-1-methyl-1H-indole-2-carboxamideHCID 18451086—

反応手順

N-[4-(4-amino-7-iodothieno[3,2-c]pyridin-3-yl)-2-methoxyphenyl]-1-methyl-1H-indole-2-carboxamide and 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carbaldehyde were reacted together according to general procedure A to furnish the title compound. LCMS (Conditions a): MH+=539.0, RT=4.10 minutes; 1H NMR (DMSO-d6, 400 MHz) δ 9.77 (s, 1 H), 9.53 (s, 1 H), 8.29 (d, J=5.3 Hz, 1 H), 7.98 (m, 2 H), 7.63 (m, 6 H), 7.36 (m, 1 H), 7.24 (s, 1 H), 7.15 (m, 1 H), 5.85 (br, 2 H), 4.04 (s, 3 H), 3.92 (s, 3 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737160B2
出典データセットuspto-grants-2010_06
ORD IDord-20733b77e8fb4fe6b651727a1012a180
出典メモuspto-grants-2010_06