Reacción #1119118

Ecuación de reacción

4-methyl-5-thiazole carboxylic acid

thionyl chloride

ethyl acetate

4-amino-1,1,3-trimethylindane

→

amorphous solid

Rendimiento 51.7%

4-methyl-N-(1,1,3-trimethylindan-4-yl)thiazole-5-carboxamide

Rendimiento 51.7%

Disolventes

triethylamine

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturawas refluxed for 1 hour
2. 2
   workup.DISTILLATIONThe reaction solution was distilled under reduced pressure
3. 3
   Otroto remove excess thionyl chloride
4. 4
   workup.DISSOLUTIONThe residue was dissolved in 10 ml of ethyl acetate
5. 5
   LavadoThe solution was washed sequentially with water, aqueous sodium hydrogen carbonate solution, water, and saturated brine
6. 6
   SecadoThe solution was dried with magnesium sulfate
7. 7
   Concentraciónconcentrated under reduced pressure
8. 8
   OtroThe concentrated residue was separated
9. 9
   Otropurified by silica gel column chromatography (eluent:ethyl acetate/n-hexane=1/2)

Procedimiento

A mixture of 1.7 g (10.3 mmols) of 4-methyl-5-thiazole carboxylic acid and 10 ml of thionyl chloride was refluxed for 1 hour. The reaction solution was distilled under reduced pressure to remove excess thionyl chloride. The residue was dissolved in 10 ml of ethyl acetate. The solution was added to 10 ml of an ethyl acetate solution of 1.8 g (10.3 mmols) of 4-amino-1,1,3-trimethylindane and 4 ml of triethylamine, and the resultant solution was stirred at room temperature for 3 hours. The solution was washed sequentially with water, aqueous sodium hydrogen carbonate solution, water, and saturated brine. The solution was dried with magnesium sulfate and then concentrated under reduced pressure. The concentrated residue was separated and purified by silica gel column chromatography (eluent:ethyl acetate/n-hexane=1/2), to obtain 1.6 g of amorphous solid substance (Compound No. 6 shown in Table 4). The yield was 50.2%.

Fuente