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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713298Generated: November 3, 2026

Dimethylformamide → 2',3',5'-Tris-O-(tert-butyldimethylsilyl)-8-(3'-methoxy-carbonylmethoxybiphenyl-4-ylmethylamino)adenosine

https://huagongshe.com/reaction/1713298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl bromoacetateHCID 60984—
Reactant2',3',5'-Tris-o-(tert-butyl-dimethylsilyl)-8-(3'-hydroxybiphenyl-4-ylmethylamino)-adenosineHCID 67455700—
Product2',3',5'-Tris-O-(tert-butyldimethylsilyl)-8-(3'-methoxy-carbonylmethoxybiphenyl-4-ylmethylamino)adenosineHCID 131728322—

Reaction Steps

To a solution of 2′,3′,5′-tris-O-(tert-butyl-dimethylsilyl)-8-(3′-hydroxybiphenyl-4-ylmethylamino)-adenosine (0.612 g) in N,N-dimethylformamide (4.0 mL) was added potassium carbonate (0.165 g). Then methyl bromoacetate (0.098 mL) was added, and the resulting mixture was stirred at room temperature for 5 hours. The reaction mixture was partitioned between diethyl ether (55 mL) and water (10 mL). The organic layer was washed successively with water (10 mL×2) and brine (10 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: hexane/ethyl acetate=3/2) to give the title compound (0.423 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795236B2
Source datasetuspto-grants-2010_09
ORD IDord-64d4311f53584cfc85c9d740afb4d1a0
Source noteuspto-grants-2010_09