Réaction #69557

Équation de réaction

tert-butyl[3-(4-hydroxy-2,6-dimethoxyphenyl)-6-methoxypyrazolo[5,1-b][1,3]thiazol-7-yl]carbamate

potassium carbonate

iodoethane

tetrahydro-4H-pyran-4-one

sodium triacetoxyborohydride

sodium hydride

1-iodopropane

→

title compound

Rendement 59.6%

3-[4-Ethoxy-2,6-dimethoxyphenyl]-6-methoxy-N-propyl-N-(tetrahydro-2H-pyran-4-yl)pyrazolo[5,1-b][1,3]thiazole-7-amine

Rendement 59.6%

Solvants

DMF

tetrahydrofuran

acetic acid

Water

Conditions de réaction

Traitement

1. 1
   Extractionthe mixture was extracted with diethyl ether
2. 2
   SéchageThe organic layer was dried over anhydrous magnesium sulfate
3. 3
   workup.DISTILLATIONthe solvent was distilled off under reduced pressure
4. 4
   workup.DISSOLUTIONThe residue was dissolved in DMF (1.88 ml)
5. 5
   workup.STIRRINGthe mixture was stirred at room temperature for 20 minutes
6. 6
   workup.ADDITIONIce was added to the reaction mixture
7. 7
   Extractionthe reaction mixture was extracted with diethyl ether
8. 8
   SéchageThe organic layer was dried over anhydrous magnesium sulfate
9. 9
   workup.DISTILLATIONthe solvent was distilled off under reduced pressure
10. 10
    workup.DISSOLUTIONThe residue was dissolved in a mixture of dichloromethane (4.69 ml) and trifluoroacetic acid (1.87 ml)
11. 11
    workup.STIRRINGthe reaction mixture was stirred at room temperature for 30 minutes
12. 12
    ConcentrationThe reaction mixture was concentrated under reduced pressure
13. 13
    workup.ADDITIONwere added
14. 14
    workup.STIRRINGthe mixture was stirred at mom temperature for 11 hours and 30 minutes
15. 15
    ConcentrationThe reaction mixture was concentrated under reduced pressure
16. 16
    workup.ADDITIONa saturated aqueous solution of sodium hydrogencarbonate was added to the residue
17. 17
    Extractionthe mixture was extracted with ethyl acetate
18. 18
    ConcentrationThe organic layer was concentrated under reduced pressure
19. 19
    Autrethe residue was purified by medium pressure silica gel column chromatography (n-heptane/ethyl acetate

Mode opératoire

To a DMF (2.97 ml) solution of tert-butyl[3-(4-hydroxy-2,6-dimethoxyphenyl)-6-methoxypyrazolo[5,1-b][1,3]thiazol-7-yl]carbamate (150 mg, 0.356 mmol) were added potassium carbonate (78.7 mg, 0.570 mmol) and iodoethane (45.6 μl, 0.570 mmol), and the mixture was stirred at room temperature for 16 hours and 10 minutes. Water was added to the reaction mixture, and the mixture was extracted with diethyl ether. The organic layer was dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. The residue was dissolved in DMF (1.88 ml), and sodium hydride (50% oil dispersion: 20.8 mg, 0.434 mmol) and 1-iodopropane (42.3 μl, 0.434 mmol) were added thereto, and the mixture was stirred at room temperature for 20 minutes. Ice was added to the reaction mixture, and the reaction mixture was extracted with diethyl ether. The organic layer was dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. The residue was dissolved in a mixture of dichloromethane (4.69 ml) and trifluoroacetic acid (1.87 ml), and the reaction mixture was stirred at room temperature for 30 minutes. The reaction mixture was concentrated under reduced pressure. The residue was dissolved in a mixture of tetrahydrofuran (11.7 ml) and acetic acid (1.17 ml), tetrahydro-4H-pyran-4-one (61.5 μl, 0.670 mmol) and sodium triacetoxyborohydride (142 mg, 0.670 mmol) were added, and the mixture was stirred at mom temperature for 11 hours and 30 minutes. The reaction mixture was concentrated under reduced pressure, a saturated aqueous solution of sodium hydrogencarbonate was added to the residue, and the mixture was extracted with ethyl acetate. The organic layer was concentrated under reduced pressure, and the residue was purified by medium pressure silica gel column chromatography (n-heptane/ethyl acetate: 10% then 50%) to obtain the title compound (101 mg, 0.212 mmol).

Source