Reaktion #2360262
ord-2babbfc45fb94c59b95100f3e80aa0e3
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1workup.ADDITIONThis mixture is then added under nitrogen to a solution
- 2workup.STIRRINGThis mixture is stirred for 2 hours at room temperature
- 3Extraktionextracted with DCM
- 4Waschenwashed once with water
- 5Trocknenwith saturated NaCl solution, and the organic phase is dried over Na2SO4
- 6FiltrationThe resulting phase is filtered
- 7Sonstigethe filtrate is evaporated under reduced pressure
- 8SonstigeThe residue is chromatographed on silica gel
- 9Wascheneluting with a DCM/MeOH mixture from (100/0 v/v) up to (100/4 v/v)
- 10SonstigeThe solid obtained
- 11Filtrationfiltered off
- 12Sonstigedried
Vorschrift
210 mg (0.51 mmol) of 4-(4-aminophenyl)-6,8,8-trimethyl-2-(8-oxa-3-azabicyclo[3.2.1]oct-3-yl)-7,8-dihydro-6H-9-oxa-1,3,6-triazabenzocyclohepten-5-one and 314.5 mg (3 mmol) of triethylamine are added to 3 ml of DCM. This mixture is then added under nitrogen to a solution containing 152.2 mg (0.51 mmol) of triphosgene in 3 ml of DCM. The mixture is stirred at room temperature for 30 minutes, and 268.1 mg (2 mmol) of 2-amino-4-methoxypyridine are then added. This mixture is stirred for 2 hours at room temperature, extracted with DCM, washed once with water and then with saturated NaCl solution, and the organic phase is dried over Na2SO4. The resulting phase is filtered and the filtrate is evaporated under reduced pressure. The residue is chromatographed on silica gel, eluting with a DCM/MeOH mixture from (100/0 v/v) up to (100/4 v/v). The solid obtained is then taken up in a DCM/MeOH/pentane mixture, filtered off and dried to give 85 mg of 1-(4-methoxypyridin-2-yl)-3-{4-[6,8,8-trimethyl-2-(8-oxa-3-azabicyclo[3.2.1]oct-3-yl)-5-oxo-5,6,7,8-tetrahydro-9-oxa-1,3,6-triazabenzocyclohepten-4-yl]phenyl}urea.