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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271261Generated: November 3, 2026

Adenosine → 9-(2-Deoxy-4-C-ethynyl-beta-D-ribo-pentofuranosyl)guanine

https://huagongshe.com/reaction/2271261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAdenosineHCID 60961—
ReactantTromethamine hydrochlorideHCID 93573—
ReactantAdenosine, 2-amino-2'-deoxy-4'-C-ethynyl-HCID 481530—
SolventWaterHCID 962—
Product9-(2-Deoxy-4-C-ethynyl-beta-D-ribo-pentofuranosyl)guanineHCID 135422917—

Reaction Conditions

Temperature40 °C

Reaction Steps

To a Tris-HCl buffer solution (7.8 ml, pH 7.5) of Compound 28 (0.03 g, 0.103 mmol), adenosine deaminase (0.057 ml, 20 unit) was added, and the mixture was stirred for 2 hours at 40° C., followed by cooling to room temperature. The reaction mixture was applied to a reverse-phase ODS silica gel column (50 g), desalted by water (500 ml) flow, and through use of aqueous 2.5% ethanol, Compound 30 was eluted. Recrystallization from water yielded Compound 30 in an amount of 0.015 g (50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06333315B1
Source datasetuspto-grants-2001_12
ORD IDord-e9fb052f6250434283070ff1b4dd46c6
Source noteuspto-grants-2001_12