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HRID 1256320作成日:2026年10月26日

1-Piperazinecarboxaldehyde → N-(7-(4-formylpiperazin-1-yl)pyrazolo[1,5-a]pyrimidin-5-yl)-4-(2-hydroxypropan-2-yl)benzamide

https://huagongshe.com/reaction/1256320

反応式

関与物質

役割名称HCID仕込み量
反応物1-PiperazinecarboxaldehydeHCID 82191—
反応物N-(7-chloropyrazolo[1,5-a]pyrimidin-5-yl)-4-(2-hydroxypropan-2-yl)benzamideHCID 86652272—
触媒Dimethyl SulfoxideHCID 679—
溶媒MethanolHCID 887—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物N-(7-(4-formylpiperazin-1-yl)pyrazolo[1,5-a]pyrimidin-5-yl)-4-(2-hydroxypropan-2-yl)benzamideHCID 8665227357%

反応手順

A solution of N-(7-chloropyrazolo[1,5-a]pyrimidin-5-yl)-4-(2-hydroxypropan-2-yl)benzamide (2D, 50 mg, 0.151 mmol) and piperazine-1-carbaldehyde (34 mg, 0.302 mmol) in NMP (0.950 mL) was stirred at 85° C. overnight. After cooling to room temperature, the mixture was diluted with a few drops of DMSO and methanol, and was then purified by preparatory HPLC, 20-45% (MeCN/H2O gradient+0.01% TFA). Lyophilization of the combined fractions gave the titled compound as a white solid (35 mg, 57%). 1H NMR (400 MHz, DMSO-d6) δ ppm 1.45 (s, 6 H) 3.59-3.82 (m, 8 H) 6.39 (d, J=2.02 Hz, 1 H) 7.43 (s, 1 H) 7.60 (d, J=8.59 Hz, 2 H) 8.00 (d, J=8.34 Hz, 2 H) 8.08-8.15 (m, 2 H) 10.94 (s, 1 H). ESI-MS: m/z 409.2 (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-c33fc80d8ed04d859a934e31b63bd7a2
出典メモuspto-grants-2013_06