HRID2092820

反应详情

EQUATION

反应方程式

HRID 2092820 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
100 °C

PROCEDURE

实验过程

To a solution of methyl 6-chloro-4-cyano-2-(1-ethyl-1H-pyrazol-4-yl)nicotinate (201 mg, 0.691 mmol) in DMF (1 mL) was added DIPEA (0.242 mL, 1.383 mmol) and tert-butyl (1S,2R)-2-aminocyclohexylcarbamate (237 mg, 1.106 mmol). The reaction mixture was stirred at 100° C. overnight, after which the solvent was removed, and the resulting crude material was diluted in MeOH (5.0 mL) and purified via reverse phase preparative HPLC. The collected fractions were collected and ACN was removed via rotary evaporation. The resulting aq solution was neutralized with saturated aq NaHCO3 and washed with EtOAc (2×200 mL), dried over Na2SO4, and filtered. The organic phase was stripped to dryness via rotary evaporation to yield the title compound (62 mg, 19%). [M+H] calc'd for C24H32N6O4, 469. found, 469.

WORKUP

后处理

  1. customafter which the solvent was removed
  2. additionthe resulting crude material was diluted in MeOH (5.0 mL)
  3. custompurified via reverse phase preparative HPLC
  4. customThe collected fractions were collected
  5. customACN was removed via rotary evaporation
  6. washwashed with EtOAc (2×200 mL)
  7. dry with materialdried over Na2SO4
  8. filtrationfiltered
  9. customThe organic phase was stripped to dryness via rotary evaporation