反应详情

温度

60 °C

To a solution of 2-methyl-2-[(1H-indazol-3-yl)methoxy]propanoic acid (26 g; 0.093 mol) in DMF (200 ml) was added 60% NaH (10 g; 0.25 mol) and the mixture was stirred for 10 minutes at 60° C. 1-chloro-1,2,3,4-tetrahydronaphthalene (0.217 mol) was then added to the mixture and the whole was stirred at 60° C. for 18 hours. The reaction was stopped by pouring the mixture into water (1 L), followed by acidifying with 5 N HCl and extracting the product with diethyl ether (3×250 ml). The residue obtained was dissolved in 95° ethanol (100 ml) and treated at reflux with 1N NaOH (200 ml) for 2 hours. The solution was then cooled to room temperature and washed with diethyl ether (3×200 ml). The alkaline phase was then acidified with concentrated HCl and extracted with ethyl acetate (3×300 ml). The combined organic phases were concentrated under reduced pressure and the crude residue obtained was purified by crystallization from ethyl acetate. 31 g of 2-methyl-2-{[1-(1,2,3,4-tetrahydronaphth-1-yl)-1H-indazol-3-yl]methoxy}-propanoic acid were thus obtained.

1. stirringthe whole was stirred at 60° C. for 18 hours
2. extractionextracting the product with diethyl ether (3×250 ml)
3. customThe residue obtained
4. additiontreated
5. temperatureThe solution was then cooled to room temperature
6. washwashed with diethyl ether (3×200 ml)
7. extractionextracted with ethyl acetate (3×300 ml)
8. concentrationThe combined organic phases were concentrated under reduced pressure
9. customthe crude residue obtained
10. customwas purified by crystallization from ethyl acetate