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HRID 272739作成日:2026年10月25日

4-Methyl-5-(2-hydroxyethyl)thiazole → 2-Bromo-4-{[2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]methyl}-1,3-thiazole

https://huagongshe.com/reaction/272739

反応式

関与物質

役割名称HCID仕込み量
反応物4-Methyl-5-(2-hydroxyethyl)thiazoleHCID 1136—
反応物4-Bromo-2-methoxyphenolHCID 262234—
反応物2-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenolHCID 2734650—
生成物2-Bromo-4-{[2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]methyl}-1,3-thiazoleHCID 69219262—

反応手順

The title compound was prepared by substituting Example 652A for 2-(4-methylthiazol-5-yl)-ethanol and 2-methoxy-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenol for 4-bromo-2-methoxyphenol, respectively, in Example 630A. MS (ESI) m/e 426 (M+H)+; 1H NMR (300 MHz, DMSO-d.6 □ 7.77 (s, 1H), 7.25 (dd, J=8.1, 1.4 Hz, 1H), 7.15 (d, J=1.4 Hz, 1H), 7.09 (d, J=8.1 Hz, 1H), 5.15 (s, 2H), 3.77 (s, 3H), 1.28 (s, 12H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07456169B2
出典データセットuspto-grants-2008_11
ORD IDord-49143dd23fa843aaab0a83b43a1e40d0
出典メモuspto-grants-2008_11