反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
A solution of N-(7-chloropyrazolo[1,5-a]pyrimidin-5-yl)-4-(2-hydroxypropan-2-yl)benzamide (2D, 200 mg, 0.604 mmol) and 4-(methoxymethyl)piperidine (117 mg, 0.906 mmol) in Dioxane (6 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, 5-95% (MeCN/H2O gradient+0.01% TFA). Lyophilization of the combined fractions gave the titled compound as a yellow solid (50 mg, 20%). 1H NMR (400 MHz, DMSO-d6) δ ppm 1.45 (s, 6 H) 1.59-1.75 (m, 2 H) 1.98-2.12 (m, 2 H) 3.31 (s, 3 H) 3.41-3.58 (m, 3 H) 3.97-4.15 (m, 2 H) 6.35 (d, J=2.27 Hz, 1 H) 7.40 (s, 1 H) 7.60 (m, J=8.34 Hz, 2 H) 7.99 (m, J=8.59 Hz, 2 H) 8.08 (d, J=2.27 Hz, 1 H) 10.88 (s, 1 H). ESI-MS: m/z 424.2 (M+H)+.
WORKUP
后处理
- customwas then purified by preparatory HPLC, 5-95% (MeCN/H2O gradient+0.01% TFA)