Chlorine → 2-Chlorohypoxanthine hydrochloride monohydrate

According to the invention, the objectives outlined above are achieved by first preparing the monohydrate of 2-chlorohypoxanthine-hydrochloride starting from commercial 2-thioxanthine by chlorination in the presence of concentrated hydrochloric acid. To do this, the 2-thioxanthine is first suspended in concentrated hydrochloric acid and chlorine is introduced into the reaction mixture over a period of 3 to 7 hours--preferably about 5 hours--at a temperature of 0° C. to 10° C.--preferably 2° C. to 7° C. and especially 3° C. to 5° C. Then some of the hydrochloric acid is distilled off and the reaction mixture is cooled to a temperature in the range from -5° C. to +10° C.--preferably 0° C. to 5° C.--to cause precipitation of the required 2-chlorohypoxanthine in the form of the monohydrate of its hydrochloric salt. The reaction mixture is then suction filtered and the crystalline residue is washed first with saline solution and then with an organic solvent, preferably an alcohol, especially isopropanol, and dried.

1. customabout 5 hours
2. customat a temperature of 0° C. to 10° C.
3. custom2° C. to 7° C. and especially 3° C. to 5° C
4. distillationThen some of the hydrochloric acid is distilled off
5. temperaturethe reaction mixture is cooled to a temperature in the range from -5° C. to +10° C.
6. custom0° C. to 5° C.
7. customprecipitation of the required 2-chlorohypoxanthine in the form of the monohydrate of its hydrochloric salt
8. filtrationsuction filtered
9. washthe crystalline residue is washed first with saline solution
10. dry with materialwith an organic solvent, preferably an alcohol, especially isopropanol, and dried

ORD record

ord-7a9181cc2f7741019519f0ef2b81447b

Source dataset

uspto-grants-1993_11

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05264573