反应 #833507

ord-bd85c211a6b04be6b06cfde35b3e5e8b

反应方程式

CN1CCCC1=O
N-methyl pyrrolidinone
O
water
O=C([O-])O.[Na+]
Sodium bicarbonate
CCOc1cc2ncc(C#N)c(Nc3ccc(F)c(Cl)c3)c2cc1N
4-[3-chloro-4-fluorophenyl]amino-6-amino-3-cyano-7-ethoxy quinoline
CCOc1cc2ncc(C#N)c(Nc3ccc(F)c(Cl)c3)c2cc1NC(=O)/C=C/CN(C)C
product
收率 86.0%
CCOc1cc2ncc(C#N)c(Nc3ccc(F)c(Cl)c3)c2cc1NC(=O)/C=C/CN(C)C
EKB-569
收率 86.0%

溶剂

反应条件

温度
42.5°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他A 3 L multi-neck flask was equipped with an agitator
  2. 2
    其他At ambient temperature
  3. 3
    workup.ADDITION6,002,008] was added
  4. 4
    温度The flask was cooled to 0-10° C
  5. 5
    其他was transferred via dip tube
  6. 6
    workup.WAITpositive nitrogen pressure to the 3 L flask over 30-45 min
  7. 7
    温度while maintaining 0-10° C
  8. 8
    其他was kept at 0-10° C. for a minimum of 2 h
  9. 9
    其他A 12 L multi-neck flask equipped with agitator
  10. 10
    workup.STIRRINGstirred until a solution
  11. 11
    其他was obtained
  12. 12
    温度The solution was cooled to 20-24° C
  13. 13
    workup.WAITpositive nitrogen pressure, to the 12 L flask over 45-60 min
  14. 14
    温度while maintaining 20-24° C
  15. 15
    温度The mixture was maintained at 20-24° C. for a minimum of 1 h
  16. 16
    过滤filtered on a Buchner funnel
  17. 17
    洗涤rinsed with water (3×0.40 kg, 3×0.40 L) with suction
  18. 18
    温度being maintained
  19. 19
    其他The product was dried in a vacuum oven at 50° C.

实验过程

A 3 L multi-neck flask was equipped with an agitator, thermometer, dip tube, and nitrogen protection. The flask was charged with N-methyl pyrrolidinone (0.77 kg, 0.75 L, d=1.033 g/mL). At ambient temperature, 4-[3-chloro-4-fluorophenyl]amino-6-amino-3-cyano-7-ethoxy quinoline (0.0748 kg) ]see, U.S. Pat. No. 6,002,008] was added and the mixture stirred while heating to 40-45° C. and hold for 15 min. The flask was cooled to 0-10° C. The mixture containing 4-N,N-dimethylaminocrotonoyl chloride hydrochloride was transferred via dip tube and positive nitrogen pressure to the 3 L flask over 30-45 min, while maintaining 0-10° C. The mixture was kept at 0-10° C. for a minimum of 2 h. The reaction was checked for completion by HPLC. The reaction is complete when there is ≦2% of the starting material (4-[3-chloro-4-fluorophenyl]amino-6-amino-3-cyano-7-ethoxy quinoline) present. A 12 L multi-neck flask equipped with agitator, thermometer, dip tube, and nitrogen protection was charged with water (2.61 kg, 2.61 L). Sodium bicarbonate (0.209 kg) was added and stirred until a solution was obtained. The solution was cooled to 20-24° C. The NMP-CH3CN mixture was transferred, via dip tube and positive nitrogen pressure, to the 12 L flask over 45-60 min, while maintaining 20-24° C. The mixture was maintained at 20-24° C. for a minimum of 1 h, and filtered on a Buchner funnel, and rinsed with water (3×0.40 kg, 3×0.40 L) with suction being maintained until dripping stops. The product was dried in a vacuum oven at 50° C. and 10 mm Hg for 28-30 h to give 78.5 g (86% yield) of product.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: USRE040418E1uspto-grants-2008_07