Formic Acid → 3-(D-glucopyranos-6-yl)-1-(2-chloroethyl)-1-nitrosourea

1.79 g (10 mmol) of 6-amino-6-deoxy-D-glucopyranose is dissolved in a mixture of 10 ml methanol and 10 ml isopropanol, and to this solution is added formic acid dropwise, with stirring, to adjust the PH of the solution to 7.8. The resulting solution is then added dropwise to a solution prepared by dissolving 3.28 g (12 mmol) of o-nitrophenyl N-(2-chloroethyl)-N-nitrosocarbamate in a mixture of 10 ml tetrahydrofuran and 10 ml ethylacetate, while stirring, at 0°-5° C. over 30 minutes. The resultant mixture is stirred at the same temperature for a further 2 hours, and the thus reacted solution is concentrated at 30° C. and below, under reduced pressure. To the oily residue produced is added ethyl ether and the solution is left at 0°-5° C. overnight. The crystalline residue obtained is washed with chloroform and further with ethyl ether, dried under reduced pressure, and recrystallized from anhydrous ethanol-n-hexane (4:1) to give 2.71 g of 3-(D-glucopyranos-6-yl)-1-(2-chloroethyl)-1-nitrosourea. Yield 86.3%. mp 102°-103° C. (decomp.). [α]D20 +55° (C 0.5, methanol; the value of +55° reduced to +31° after 22 hours).

1. additionThe resulting solution is then added dropwise to a solution
2. customprepared
3. stirringwhile stirring, at 0°-5° C. over 30 minutes
4. concentrationthe thus reacted solution is concentrated at 30° C.
5. customTo the oily residue produced
6. customThe crystalline residue obtained
7. washis washed with chloroform and further with ethyl ether
8. customdried under reduced pressure
9. customrecrystallized from anhydrous ethanol-n-hexane (4:1)

ORD record

ord-70dff31b371845499247e7ded2d694dd

Source dataset

uspto-grants-1979_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04156777