HRID1176029

反应详情

EQUATION

反应方程式

HRID 1176029 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To 2,4-Dichloro-6-piperidin-1-yl-quinazoline (100 mg, 0.365 mmol), in ethanol (5 omL) was added 5-Cyclopropyl-2H-pyrazol-3-ylamine (88 mg 0.71 mmol). The additional resulted in the formation of a white precipitate. The partial solution was stirred for 10 hr and (2-Chloro-6-piperidin-1-yl-quinazolin-4-yl)-(5-cyclopropyl-2H-pyrazol-3-yl)-amine was colleted by filtration to give 80 mg (61% yield). HPLC tr=4.90 min (100%), LCMS m/e 369.31 (M+H), 367.28 (M-H) tr=3.41 min, HNMR (500 MHz, dmso): 12.30-12.25 (1H, bs), 10.67 (1H, s), 7.80-7.85 (1H, s), 7.65 91H, d), 7.50 (1H, d), 6.50 (1H, bs), 3.40 (4H, m0, 2.90 (1H, m), 1.70-1.55 (6H, m), 0.95 (2H, m), 0.70 (2H, m).

WORKUP

后处理

  1. customThe additional resulted in the formation of a white precipitate
  2. filtration(2-Chloro-6-piperidin-1-yl-quinazolin-4-yl)-(5-cyclopropyl-2H-pyrazol-3-yl)-amine was colleted by filtration
  3. customto give 80 mg (61% yield)
  4. customHPLC tr=4.90 min (100%), LCMS m/e 369.31 (M+H), 367.28 (M-H) tr=3.41 min, HNMR (500 MHz, dmso): 12.30-12.25 (1H, bs), 10.67 (1H, s), 7.80-7.85 (1H, s), 7.65 91H