تفاعل #590111

معادلة التفاعل

K2CO3

allyl bromide

2-(tert-Butoxycarbonyl)amino-5-trifluoromethylbenzoic acid

DMF

EtOAc

→

title compound

2-(3-Isopropyl-ureido)-5-trifluoromethyl-benzoic acid

المذيبات

water

ظروف التفاعل

المعالجة

1. 1
   workup.ADDITIONwere added
2. 2
   غسيلThe organic layer was washed with brine
3. 3
   أخرىdried
4. 4
   ترشيحfiltered
5. 5
   تركيزconcentrated (2.05 g)
6. 6
   workup.DISSOLUTIONThe resulting material was dissolved in CH2Cl2 (4 mL)
7. 7
   تركيزthe solution was concentrated
8. 8
   workup.DISSOLUTIONThis material was dissolved in THF
9. 9
   workup.ADDITIONadded dropwise to a THF (50 mL) solution of trichloromethyl chloroformate (1.9 mL)
10. 10
    تركيزthe solution was concentrated
11. 11
    workup.ADDITIONa THF (30 mL) solution of iso-propylamine (4.3 mL) was added
12. 12
    workup.WAITAfter 18 h
13. 13
    workup.ADDITIONthe solution was diluted with EtOAc
14. 14
    غسيلwas washed with brine solution and 1N HCl
15. 15
    تجفيفThe organic layer was dried (MgSO4)
16. 16
    ترشيحfiltered
17. 17
    تركيزconcentrated to a white solid
18. 18
    workup.DISSOLUTIONThis solid was dissolved in CH3CN (22 mL)
19. 19
    workup.ADDITIONto the addition of pyrrolidine (0.41 mL) and Pd(PPh)4 (105 mg)
20. 20
    workup.WAITAfter 18 h
21. 21
    workup.ADDITIONthe solution was diluted with EtOAc
22. 22
    غسيلwas washed 1N HCl
23. 23
    تجفيفThe organic layer was dried (MgSO4)
24. 24
    ترشيحfiltered
25. 25
    تركيزconcentrated

الإجراء التجريبي

2-(tert-Butoxycarbonyl)amino-5-trifluoromethylbenzoic acid (2 g) was dissolved in DMF prior to the addition of K2CO3 (1.08 g) and allyl bromide (0.68 mL). The mixture was stirred for 18 h before EtOAc and water were added. The organic layer was washed with brine, dried, filtered, and concentrated (2.05 g). The resulting material was dissolved in CH2Cl2 (4 mL) and TFA (4 mL). After 1 h, the solution was concentrated. This material was dissolved in THF and added dropwise to a THF (50 mL) solution of trichloromethyl chloroformate (1.9 mL). After stirring for 18 h, the solution was concentrated and a THF (30 mL) solution of iso-propylamine (4.3 mL) was added. After 18 h, the solution was diluted with EtOAc and was washed with brine solution and 1N HCl. The organic layer was dried (MgSO4), filtered, and concentrated to a white solid. This solid was dissolved in CH3CN (22 mL) prior to the addition of pyrrolidine (0.41 mL) and Pd(PPh)4 (105 mg). After 18 h, the solution was diluted with EtOAc and was washed 1N HCl. The organic layer was dried (MgSO4), filtered, and concentrated to give the title compound (1.1 g) as a white solid: 1H NMR (DMSO, δppm, 300 mHz) 1.11 (d, 6H), 3.78 (m, 1H), 7.63 (br d, 1H), 7.81 (dd, 1H), 8.14 (d, 1H), 8.64 (d, 1H), 10.27 (s, 1H), 13.83 (br s, 1H).

المصدر