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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186324Generated: October 31, 2026

Trimethylsilyl triflate → HCID 10746734, compound

https://huagongshe.com/reaction/2186324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl triflateHCID 65367—
Reactant7h-purine-2,8-diamineHCID 243948—
ReactantSodium BicarbonateHCID 516892—
ReactantN,O-bis(trimethylsilyl)acetamideHCID 6913588—
ReactantHCID 12042250HCID 12042250—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 10746734HCID 10746734—

Reaction Steps

To a solution of Compound 6 (1.1 g, 2 mmol) in 1,2-dichloroethane (16.5 ml), diaminopurine (0.45 g, 3 mmol) and N,O-bis(trimethylsilyl)acetamide (4.4 ml, 18 mmol) were added, followed by refluxing for three hours. After the mixture was cooled to room temperature, trimethylsilyl trifluoromethanesulfonate (0.77 ml, 4 mmol) was added dropwise to the mixture at 0° C. in an argon atmosphere. The mixture was stirred for 15 minutes at room temperature, refluxed for 24 hours, and cooled to room temperature. A saturated aqueous solution of sodium hydrogencarbonate was added thereto at 0° C., followed by stirring for 15 minutes at room temperature. Insoluble materials were separated through filtration by use of Celite, and then the organic layer was separated from the filtrate. After an aqueous layer was extracted with chloroform once, the organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was applied to a silica gel column (20 g, eluent; ethyl acetate:n-hexane:ethanol=20:10:1), to thereby yield Compound 25 in an amount of 0.85 g (66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403568B1
Source datasetuspto-grants-2002_06
ORD IDord-d1d8deba24fc4bfabe0b449243a2abc6
Source noteuspto-grants-2002_06