反应详情

温度

50 °C

A mixture of 1.05 g (5 mmol) 3-Chloro-1H-indole-5-carboxylic acid methyl ester and 1.05 g (25 mmol) LiOH.H2O in THF, methanol, water was stirred at 50° C. for 4 h. The mixture was evaporated to dryness and the corresponding acid was used without further purification in the subsequent step. 0.77 g (6 mmol) 1-(2-propyl)-piperazine, 2.4g (7.5 mmol) TBTU, 2.5 g (25 mmol) NEt3 and 20 mL DMF was added and the mixture was stirred at room temperature for 4 h. 1N NaHCO3 was added and the mixture was extracted with DCM. The combined organic layers were dried with MgSO4, filtered and evaporated. The residue was purified by flash column chromatography on silica eluting with a gradient formed from heptane, ethyl acetate, methanol and NEt3. The combined product fractions were evaporated to yield 0.67 g (44%) of the title compound as light brown solid. MS(m/e): 306.3 (MH+).

1. customThe mixture was evaporated to dryness
2. customthe corresponding acid was used without further purification in the subsequent step
3. stirringthe mixture was stirred at room temperature for 4 h
4. extractionthe mixture was extracted with DCM
5. dry with materialThe combined organic layers were dried with MgSO4
6. filtrationfiltered
7. customevaporated
8. customThe residue was purified by flash column chromatography on silica eluting with a gradient
9. customformed from heptane, ethyl acetate, methanol and NEt3
10. customThe combined product fractions were evaporated