Hydrochloric Acid → Olanzapine

温度

100 °C

A suspension of 2,4-bis(4-methyl-1-piperazinyl)-3-propylidene-3H-[1,5]benzodiazepine (11.90 g, 31.3 mmol), sulphur (20.07 g, 626 mmol) and triethyl amine (4.34 ml, 31.3 mmol) in dimethyl sulfoxide (100 ml) and 1-propanol (100 ml) was heated at 100° C. for five days. The resulting black suspension was cooled and filtered off and the filtrate was evaporated at reduced pressure to obtain a viscous black oil. Dichloromethane (600 ml) and HCl (0.2 M, 600 ml) were added and the phases were separated. The organic phase was extracted again with HCl (0.5 M, 100 ml). The combined water phases were made alkalic at a pH of 9 to 10. Dark brown precipitate was filtered off. Dichloromethane (250 ml) was added to the filtrate. The phases were separated and the water phase was extracted with dichloromethane (2×60 ml). The organic phase was dried over anhydrous Na2SO4 and the solvent was evaporated at reduced pressure. The black oil was combined with precipitate and purified by chromatography on silica gel, eluted with ethyl acetate/triethylamine 50/1 to obtain 1.195 g (12%) of the title product.

1. temperatureThe resulting black suspension was cooled
2. filtrationfiltered off
3. customthe filtrate was evaporated at reduced pressure
4. customto obtain a viscous black oil
5. customthe phases were separated
6. extractionThe organic phase was extracted again with HCl (0.5 M, 100 ml)
7. filtrationDark brown precipitate was filtered off
8. additionDichloromethane (250 ml) was added to the filtrate
9. customThe phases were separated
10. extractionthe water phase was extracted with dichloromethane (2×60 ml)
11. dry with materialThe organic phase was dried over anhydrous Na2SO4
12. customthe solvent was evaporated at reduced pressure
13. custompurified by chromatography on silica gel
14. washeluted with ethyl acetate/triethylamine 50/1

ORDレコード

ord-9507b3ebe976448097f8f383c6174f7a

出典データセット

uspto-grants-2009_03

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07498433B2