Reaktion #159988
ord-f5e3b4d898c04fed87046d3ce1e0178b
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1FiltrationThe separated organic layer was filtered over silica gel
- 2Einengenthe filtrate was concentrated
- 3SonstigeThe residue was purified by FCC (petroleum ether/Et2O)
- 4SonstigeThe product fractions were collected
- 5Sonstigethe solvent was evaporated
- 6workup.DISSOLUTIONThis residue was dissolved in TFA/DCM/water (5:12:1, 12 mL)
- 7workup.STIRRINGstirred at rt for 90 min
- 8EinengenThe mixture was concentrated
- 9workup.ADDITIONresidue was diluted with 1 M NaOH
- 10Extraktionextracted with DCM (2×)
- 11WaschenThe combined organic layers were washed with satd
- 12TrocknenNaCl, dried
- 13Einengenconcentrated
- 14SonstigeThe residue was recrystallized from 2-propanol
Vorschrift
A mixture of 2-(1,1-dioxo-1λ6-thiomorpholin-4-yl)-4 trifluoromethanesulfonyloxy-5,6,8,9-tetrahydro-pyrimido[4,5-d]azepine-7-carboxylic acid tert-butyl ester (0.0008 mol), (4-methylphenyl)-boronic acid (0.0008 mol), Pd(dppf)Cl2 (0.00008 mol) and K2CO3 (0.0016 mol) in 2-propanone/toluene/water (4:4:1, 8 mL) was stirred in a microwave for 30 min at 130° C. The separated organic layer was filtered over silica gel and the filtrate was concentrated. The residue was purified by FCC (petroleum ether/Et2O). The product fractions were collected and the solvent was evaporated. This residue was dissolved in TFA/DCM/water (5:12:1, 12 mL) and stirred at rt for 90 min. The mixture was concentrated and residue was diluted with 1 M NaOH and extracted with DCM (2×). The combined organic layers were washed with satd. NaCl, dried, and concentrated. The residue was recrystallized from 2-propanol to give 0.190 g (64%) of the title compound.