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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836253Generated: October 26, 2026

Hydrogen Bromide → HCID 87285362, compound

https://huagongshe.com/reaction/1836253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantSodiumHCID 5360545—
Reactant3,5-Bis-o-(2,4-dichlorobenzyl)-2-c-vinyl-1-o-methyl-alpha-d-ribofuranoseHCID 67142896—
ReactantHCID 178418725HCID 178418725—
SolventDichloromethaneHCID 6344—
Solvent7-Deaza-2'-C-methyladenosineHCID 3011893—
ProductHCID 87285362HCID 8728536222.1%

Reaction Steps

To a solution of the compound from Step A (6.4 g, 12.6 mmol) in anhydrous dichloromethane (150 mL) at −20° C. was added HBr (30% solution in AcOH, 20 mL, 75.6 mmol) dropwise. The resulting solution was stirred between −10° C. and 0° C. for 4 h, evaporated in vacuo and co-evaporated with anhydrous toluene (3×40 mL). The oily residue was dissolved in anhydrous acetonitrile (100 mL) and added to a solution of the sodium salt of 4-chloro-1H-pyrrolo[2,3-d]pyrimidine (5.8 g, 37.8 mmol) in acetonitrile (generated in situ as described in Example 62) at −20° C. The resulting mixture was allowed to come to room temperature and stirred at room temperature for 24 h. The mixture was then evaporated to dryness, taken up in water and extracted with EtOAc (2×300 mL). The combined extracts were dried over Na2SO4, filtered and evaporated. The crude mixture was purified by flash chromatography (SiO2, 10% EtOAc in hexanes) and the title compound (1.75 g) isolated as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777395B2
Source datasetuspto-grants-2004_08
ORD IDord-8830dc739fa84a71a8c708d2f8a26428
Source noteuspto-grants-2004_08