HRID1363603

反应详情

EQUATION

反应方程式

HRID 1363603 的结构方程式

CONDITIONS

反应条件

温度
90 °C

PROCEDURE

实验过程

1-[(4-Amino-2-methyl-1H-imidazo[4,5-c]quinolin-1-yl)methyl]cyclobutanol was prepared according to the general methods of Example 57 using 4-chloro-3-nitroquinoline in lieu of 4-chloro-3-nitronaphthyridine and 1-(aminomethyl)cyclobutanol in lieu of 1-(aminomethyl)cyclohexanol in Part A and trimethylorthoacetate in lieu of trimethylorthobutyrate in Part C. The crude product was triturated sequentially with ethyl acetate, hot chloroform, and acetonitrile, purified by HPFC eluting with a gradient of 0-40% CMA in chloroform, and then suspended in water (100 mL). Concentrated hydrochloric acid (2 mL) was added and the mixture was heated to 90° C. The hot solution was made basic (pH 10) with solid sodium bicarbonate. The solution was allowed to cool to ambient temperature. A precipitate was isolated by filtration, washed well with water, and then dried to provide pure product as a white powder, mp>250.0° C. Anal. Calcd for C16H18N4O C, 68.06; H, 6.43; N, 19.84. Found: C, 67.99; H, 6.54; N, 19.81.

WORKUP

后处理

  1. customThe crude product was triturated sequentially with ethyl acetate, hot chloroform, and acetonitrile
  2. custompurified by HPFC
  3. washeluting with a gradient of 0-40% CMA in chloroform
  4. additionConcentrated hydrochloric acid (2 mL) was added
  5. temperatureto cool to ambient temperature
  6. customA precipitate was isolated by filtration
  7. washwashed well with water
  8. customdried
  9. customto provide pure product as a white powder, mp>250.0° C