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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212472Generated: October 31, 2026

Water → HCID 15476591, compound

https://huagongshe.com/reaction/2212472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylamine, hydrochlorideHCID 10473—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 21049355HCID 21049355—
SolventPyridineHCID 1049—
ProductHCID 15476591HCID 1547659167%

Reaction Steps

2-amino-chloro-9-(2′,3′,5′-tri-O-acetyl-β-D-ribofuranosyl)purine (1) [M. J. Robins and B. Uznanski, Can. J. Chem., 59, 2601-2607 (1981)1(18.6 mmol, 7.96 g) was dehydrated three times azeotropically with anhydrous pyridine, and dissolved in anhydrous pyridine (180 ml), then dimethylamine hydrochloride (55.8 mmol, 4.55 g) and diisopropylethylamine (74.4 mmol, 12.9 ml) were added thereto with stirring at room temperature. The mixture was stirred at room temperature for 15 hours. After confirming completion of the reaction by TLC, water was added to the reaction mixture and concentrated in vacuo. Chloroform was added to the residue, and the organic layer was washed 3 times with water, 2 times with 5% aqueous sodium hydrogen carbonate, once with water and 2 times with 10% aqueous citrate solution, then the organic layer was dried with magnesium sulfate, and dried in vacuo after filtration. The residue was treated with azeotropic distillation with toluene until no odor of pyridine was noted, the product was purified by silica-gel chromatography (dichloromethane-ethanol) to obtain the product (2) 5.42 g (12.4 mmol) (67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101992B1
Source datasetuspto-grants-2006_09
ORD IDord-212b1b1dd8194f4fabcf85f77a2f1be4
Source noteuspto-grants-2006_09