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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905363Generated: October 26, 2026

Acetonitrile → 2-Methyladenosine

https://huagongshe.com/reaction/1905363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant5-amino-1-beta-D-ribofuranosyl-4-cyanoimidazoleHCID 10977550—
SolventAmmonia methanolHCID 21705897—
Product2-MethyladenosineHCID 45989035.9%

Reaction Conditions

Temperature180 °C

Reaction Steps

10 g of 5-amino-1-β-D-ribofuranosyl-4-imidazolecarbonitrile was dissolved in 20% ammonia methanol solution. 10 ml of acetonitrile was added thereto and the solution was heated for 5 hours at 180° C. The solvent was distilled off, purified by silica gel column chromatography and recrystallized from methanol to give 4.2 g of 2-methyladenosine (yield: 35.9%). 2-methyladenosine was methylated in the same manner as the above-mentioned [METHOD 1] to give Compound 5 and Compound 6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04843066
Source datasetuspto-grants-1989_06
ORD IDord-ad34449c2e004f64811a41dcface1a3e
Source noteuspto-grants-1989_06