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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448531Generated: November 2, 2026

HCID 22803039, compound → HCID 22803036, compound

https://huagongshe.com/reaction/1448531

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22803039HCID 22803039—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 22803036HCID 2280303657.4%

Reaction Steps

Methyl 2,6-dideoxy-2-(N'-methyl-ureido)-β-D-glucopyranoside (124 mg) of the formula: ##STR35## was dissolved in a mixture of 0.5 ml of glacial acetic acid and 2.5 ml of water, and the resulting solution was admixed with 55 mg of sodium nitrite at ambient temperature and under agitation to effect the nitrosation. The reaction mixture so obtained was then allowed to stand overnight in a refrigerator, so that a crystalline product was deposited. This crystalline product was collected by filtration and then washed with ethanol, affording 80 mg of methyl 2,6-dideoxy-2-(N'-methyl-N'-nitroso-ureido)-β-D-glucopyranoside as the desired product. The mother liquor was then treated with Amberlite IR-120 (H+ form) to remove the sodium ion, and the mother liquor so treated was concentrated by distilling off the solvent under reduced pressure. Crystallization of the residue from ethanol gave 45 mg of the desired product as a second crop. Yield 125 mg (90%). [α]D28 -14° (c 0.52, H2O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04180655
Source datasetuspto-grants-1979_12
ORD IDord-8527bb0386f84ede852663ff01975824
Source noteuspto-grants-1979_12