Reaktion #7302
ord-ad2378e8729f43cdb3501b2c8a8ba400
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Sonstigeto give 20 kg dispersion
- 2workup.DISSOLUTIONdissolved under ice-
- 3Temperaturcooling
- 4Sonstigeto prepare a charge solution
- 5FiltrationThereafter, the solution was aseptically filtered through a 0.2 μm membrane
- 6Filtrationfilter (MCGL20S03, 0.2 μm, Millipore)
- 7Sonstigeequipped with a jacket)
- 8workup.STIRRINGThen, the crystallization tank was stirred
- 9Sonstigeby bubbling with nitrogen at 0 to 15° C.
- 10workup.ADDITION25 L isopropyl alcohol was aseptically added
- 11SonstigeAfter crystallization, 55 L isopropyl alcohol
- 12workup.ADDITIONwas added aseptically
- 13workup.ADDITIONadded
- 14Filtrationthe precipitated crystals were collected aseptically by filtration
- 15WaschenThe crystals were washed with isopropyl alcohol and acetone
- 16Sonstigedried in a nitrogen stream with regulated humidity (20 to 40 RH %) for 10 hours or more
Vorschrift
Water for injection was added to 2000 g titer equivalent amount of novel non-aseptic carbapenem hydrochloride derivative to give 20 kg dispersion. This dispersion was stirred and dissolved under ice-cooling to prepare a charge solution. Thereafter, the solution was aseptically filtered through a 0.2 μm membrane filter (MCGL20S03, 0.2 μm, Millipore) and fed to a crystallization tank (equipped with a jacket). Then, the crystallization tank was stirred by bubbling with nitrogen at 0 to 15° C., and 25 L isopropyl alcohol was aseptically added thereto. After crystallization, 55 L isopropyl alcohol was added aseptically added thereto over 1 hour or so. After aging for a predetermined time, the precipitated crystals were collected aseptically by filtration. The crystals were washed with isopropyl alcohol and acetone, and dried in a nitrogen stream with regulated humidity (20 to 40 RH %) for 10 hours or more, to give novel aseptic carbapenem hydrochloride trihydrate crystals.