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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552751Generated: November 2, 2026

Ammonia → HCID 67164793, compound

https://huagongshe.com/reaction/552751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant4-Bromobenzoyl chlorideHCID 68515—
Reactant2',3'-O-IsopropylideneadenosineHCID 2723654—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductHCID 67164793HCID 6716479349%

Reaction Conditions

Temperature0 °C

Reaction Steps

[(3aR,4R,6R,6aR)-6-(6-amino-9H-purin-9-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl]methanol (0.400 g, 1.30 mmol) was dried by co-evaporation with pyridine, then suspended in dry pyridine (6.5 mL). TMSCl (0.330 mL, 2.60 mmol) was added and the mixture was stirred for 15 min. 4-Bromobenzoylchloride (0.342 g, 1.56 mmol) was added to the mixture and stirred for 2 h. The solution was cooled to 0° C. and 1 mL of H2O was added. After 5 min a 29% NH3 aq solution (0.847 mL) was added and the reaction mixture was stirred for 30 min while warming to r.t. The mixture was then concentrated and the residue was diluted with H2O (40 mL). The product was extracted with EtOAc (60 mL) and concentrated. The crude material was purified by flash chromatography (65 to 100% EtOAc/hexanes) to afford the title compound (0.305 g, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951810B2
Source datasetuspto-grants-2011_05
ORD IDord-bb4517ba29a748ebb3d3a55c4b8145aa
Source noteuspto-grants-2011_05