Reacción #51227

Ecuación de reacción

N-benzyloxycarbonyl-trans-4-[(5-hydroxylmethyl-2-isoindolinyl)carbonyl]cyclohexylamine

triethylamine

methanesulfonyl chloride

chloride

→

trans-4-[(5-morpholinomethyl-2-isoindolinyl)carbonyl]cyclohexylamine

Disolventes

Water

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturacooling
2. 2
   Temperaturacooling for 1 hour
3. 3
   Extracciónthe mixture was extracted with ethyl acetate
4. 4
   SecadoAfter the extract was dried over sodium sulfate
5. 5
   Otrothe solvent was removed under reduced pressure
6. 6
   workup.ADDITIONTo the residue were added 5 ml of dimethylformamide and 0.25 ml of morpholine
7. 7
   workup.STIRRINGthe mixture was stirred at room temperature overnight
8. 8
   workup.ADDITIONWater was added to the reaction mixture
9. 9
   Extracciónthe mixture was extracted with ethyl acetate
10. 10
    SecadoAfter the extract was dried over anhydrous sodium sulfate
11. 11
    Otrothe solvent was removed under reduced pressure
12. 12
    OtroThe residue was purified by silica gel chromatography (solvent: chloroform-methanol=100:1)
13. 13
    workup.ADDITIONThis compound was treated with palladium-carbon under hydrogen atmosphere

Procedimiento

0.15 ml of triethylamine and 0.07 ml of methanesulfonyl chloride were added to 10 ml of a tetrahydrofuranmethylene chloride suspension containing 0.31 g of N-benzyloxycarbonyl-trans-4-[(5-hydroxylmethyl-2-isoindolinyl)carbonyl]cyclohexylamine under ice-cooling, and the mixture was stirred under ice-cooling for 1 hour. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. After the extract was dried over sodium sulfate, the solvent was removed under reduced pressure. To the residue were added 5 ml of dimethylformamide and 0.25 ml of morpholine, and the mixture was stirred at room temperature overnight. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. After the extract was dried over anhydrous sodium sulfate, the solvent was removed under reduced pressure. The residue was purified by silica gel chromatography (solvent: chloroform-methanol=100:1). This compound was treated with palladium-carbon under hydrogen atmosphere to obtain trans-4-[(5-morpholinomethyl-2-isoindolinyl)carbonyl]cyclohexylamine (Reference Example 13-24 in Table 8).

Fuente