A kind of preparation method of beta configuration gemcitabine hydrochloride intermediate
A technology for gemcitabine hydrochloride and intermediates, applied in the field of drug synthesis, can solve the problems of poor reaction selectivity, cumbersome post-processing steps, affecting the yield and purity of target products, etc., and achieve the effect of improving conversion rate, simple operation and post-processing steps
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0037] A preparation method of a beta configuration gemcitabine hydrochloride intermediate, the steps are as follows:
[0038] 3g α configuration content higher gemcitabine hydrochloride intermediate II ', 20g (molar weight 0.044mol) gemcitabine hydrochloride intermediate I, 22.4g (molar weight 0.088mol) silanized cytosine dropped into 170g toluene together, 120 ℃ for 6 hours; after the reaction, slowly add the reaction solution to 160 g of absolute ethanol that has been cooled to 15 ℃, stir and crystallize at 25 ℃ for 0.5 hours, filter; the obtained filter cake is washed with 6 wt% dilute hydrochloric acid, returned to alkali (neutralized by 10% aqueous sodium hydroxide solution), dried to obtain gemcitabine hydrochloride intermediate II in β configuration; the mother liquor obtained by filtration was concentrated until a large amount of solids were precipitated, cooled to 5° C. for crystallization, filtered, and dried to obtain 3.02 g of gemcitabine hydrochloride in α configu...
Embodiment 2
[0041] Put 2.5g of gemcitabine hydrochloride intermediate II' with higher alpha configuration content, 20g (molar weight 0.044mol) gemcitabine hydrochloride intermediate I, 22.4g (molar weight 0.088mol) silanized cytosine into 170g of toluene, React at 120°C for 6h; after the reaction, slowly add the reaction solution to 160g of absolute ethanol that has been cooled to 14°C, stir and crystallize at 26°C for 0.5 hour, filter; the obtained filter cake is washed with 6wt% dilute hydrochloric acid, returned to Alkali (neutralized by 10% aqueous sodium hydroxide solution), dried to obtain gemcitabine hydrochloride intermediate II in β configuration; the mother liquor obtained by filtration was concentrated until a large amount of solids were precipitated, cooled to 6°C for crystallization, filtered, and dried to obtain 2.92 g of hydrochloric acid in α configuration Gemcitabine intermediate II' (purity 95.89wt%), the obtained α-configuration gemcitabine hydrochloride intermediate II'...
Embodiment 3
[0044]Put 2.5g of gemcitabine hydrochloride intermediate II' with higher alpha configuration content, 20g (molar weight 0.044mol) gemcitabine hydrochloride intermediate I, 22.4g (molar weight 0.088mol) silanized cytosine into 170g of toluene, React at 130°C for 6 hours; after the reaction, slowly add the reaction solution to 160g of absolute ethanol that has been cooled to 13°C, stir and crystallize at 28°C for 0.5 hours, and filter; the obtained filter cake is washed with 6wt% dilute hydrochloric acid, returned to Alkali (neutralized by 10% aqueous sodium hydroxide solution), dried to obtain the β-configuration gemcitabine hydrochloride intermediate II; the mother liquor obtained by filtration was concentrated until a large amount of solids were precipitated), cooled to 5°C for crystallization, filtered, and dried to obtain 2.85 g of the α-configuration Gemcitabine hydrochloride intermediate II' (purity 95.5wt%), the obtained α-configuration gemcitabine hydrochloride intermedi...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


