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HRID 1256330作成日:2026年10月25日

1,4-Dioxane → 4-(2-hydroxypropan-2-yl)-N-(2-methyl-7-phenylpyrazolo[1,5-a]pyrimidin-5-yl)benzamide

https://huagongshe.com/reaction/1256330

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-DioxaneHCID 31275—
反応物Phenylboronic AcidHCID 66827—
反応物N-(7-chloro-2-methylpyrazolo[1,5-a]pyrimidin-5-yl)-4-(2-hydroxypropan-2-yl)benzamideHCID 86652267—
溶媒MethanolHCID 887—
生成物4-(2-hydroxypropan-2-yl)-N-(2-methyl-7-phenylpyrazolo[1,5-a]pyrimidin-5-yl)benzamideHCID 6706442825.3%

反応条件

温度110 °C

反応手順

A suspension of N-(7-chloro-2-methylpyrazolo[1,5-a]pyrimidin-5-yl)-4-(2-hydroxypropan-2-yl)benzamide (2F, 49 mg, 0.142 mmol), phenylboronic acid (23 mg, 0.189 mmol), and [1,1′-bis[1,1′-Bis(diphenylphosphino)ferrocene]-dichloropalladium(II) (9.3 mg, 13 mmol) in 2:1 1,4-dioxane/saturated aqueous NaHCO3 (0.76 mL of 1,4-dioxane and 0.38 mL of saturated aqueous NaHCO3) was prepared in a 10 mL microwave reaction vessel and the sealed reaction vessel warmed to 110° C. for 10 minutes in a CEM microwave reactor. The reaction mixture was cooled to rt, diluted with methanol, filtered, and purified via preparative HPLC (65-75% MeCN/H2O+0.01% TFA). Lyophilization of the combined fractions gave the titled compound as a yellow solid (13.9 mg, 25%). Decomposition observed at 199.8° C. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.46 (s, 6 H), 2.40 (s, 3 H), 5.20 (br. s., 1 H), 6.40 (s, 1 H), 7.58-7.66 (m, 5 H), 7.97 (s, 1 H), 8.02 (d, J=8.59 Hz, 2 H), 8.06 (dd, J=6.57, 3.03 Hz, 2 H), 11.20 (s, 1 H); ESI-MS: m/z 387.2 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08461163B2
出典データセットuspto-grants-2013_06
ORD IDord-17db305823be411ea1e6c902f6c6811e
出典メモuspto-grants-2013_06